Peer-Reviewed Papers in Professional Journals 1. 161(5 ... · Peer-Reviewed Papers in Professional...
Transcript of Peer-Reviewed Papers in Professional Journals 1. 161(5 ... · Peer-Reviewed Papers in Professional...
List of Publications
Anthony S. Luder 015573801 December 2014
Peer-Reviewed Papers in Professional Journals
Basic Research
1. Luder AS, Greene C. Maternal phenylketonuria: Implications for medical practice in
the United States. American Journal of Obstetrics and Gynecology 1989(Nov);
161(5):1102- 1105
IF: 3.46, Rank 8/75 (Obstetrics and Gynaecology), Contribution A,C,D
2. Parker WD, Boyson SJ, Luder AS, Parks J. Evidence for a defect in NADH:ubiquinone
oxidoreductase (complex I) in Huntington's disease. Neurology 1990(Aug); 40:1231-
1233
IF: 8.017, Rank 4/185 (Clinical Neurology), Contribution A,B,C,D
3. Luder AS, Parks J, Frerman F, Parker WD. Inactivation of alpha-ketoglutarate
dehydrogenase by valproic acid and valproic acid metabolites: possible mechanism of
anti-convulsant and toxic actions. Journal of Clinical Investigation 1990(Nov);
86:1574-1581
IF: 14.152, Rank 3/106 (Medicine, Research and Experimental), Contribution A,B,C,D
4. Blom J, Davidson A, Kinkelstein JD, Luder AS, Bernadini I, Martin JJ, Tangerman A,
Trijbels FMF, Mudd SH, Goodman SI, Gahl WA. Persistent hypermethioninemia with
dominant inheritance. Journal of Inherited Metabolic Disease 1992; 15(2):188-197
IF: 3.088, Rank 36/116 (Endocrinology and Metabolism), 46/156 (Genetics and
Heredity) Contribution A,B,C,D
5. Mandel H, Espeel M, Roels F, Sofer N, Luder AS, Iancu TC, Aizin A, Berant M,
Wanders RJ Schutgens RB. A new type of peroxisomal disorder with variable
expression in liver and fibroblasts. Journal of Pediatrics 1994(Oct); 125(4):549-555
IF: 4.042, Rank 3/107 (Pediatrics), Contribution B,C,D
6. Luder AS, Barash V. Complex I deficiency with diabetes, Fanconi syndrome and
mtDNA deletion. Journal of Inherited Metabolic Disease 1994; 17(3):298-300
IF: 3.088, Rank 36/116 (Endocrinology and Metabolism), 46/156 (Genetics and
Heredity) Contribution A,B,C,D
7. Tamary H, Fromovich Y, Shalmon L, Reich Z, Dym O, Lamir N, Brenner B, Paz M, Luder
AS. Ala244Val is a common, probably ancient mutation causing factor VII deficiency
in Moroccan and Iranian Jews. Thrombosis and Haemostasis 1996(Sep); 76(3):283-
291
IF: 4.7012, Rank 9/66 (Peripheral Vascular Disease), 13/65 (Hematology),
Contribution A,C,D
8. Bercovich D, Regev Z, Ratz T, Luder A, Plotsky Y, Gruenbaum Y. Quantitative ratio of
primer pairs and annealing temperature affecting PCR products in duplex
amplification. Biotechniques. 1999 Oct;27(4):762-4, 766-8, 770.
IF: 2.55, Rank 33/71 (Biochemical Research Methods), Contribution A,D
9. Shatzky S, Moses S, Levy J, Pinsk V, Hershkovitz E, Herzog L, Shorer Z, Luder A, Parvari
R. Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic
heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and
results of nerve conduction studies. American Journal of Medical Genetics
2000(Jun); 92(5): 353-60
IF: 2.505, Rank 77/156 (Genetics and Heredity), Contribution A,B,D
10. Barbara Schenk, Timo Imbach, Christian G. Frank, Claudia E. Grubenmann, Gerald V.
Raymond, H. Hurvitz, A. Raas-Rotschild, Anthony S. Luder, Jaak Jaeken, Eric G.
Berger, Gert Matthijs, Thierry Hennet and Markus Aebi. MPDU1 mutations underlie a
novel human congenital disorder of glycosylation, designated type If. Journal of
Clinical Investigation 2001(December) 108(11); 1687-1695
IF: 14.152, Rank 3/106 (Medicine, Research and Experimental), Contribution A,B,C,D
11. Amirav I, Balanov I, Gorenberg M, Luder AS, Newhouse MT, Groshar D. ß-agonist
aerosol distribution in respiratory syncytial virus bronchiolitis in infants. Journal
Nuclear Medicine 2002 43; 487-491
IF: 7.022, Rank 1/111 (Radiology, Nuclear Medicine & Medical Imaging),
Contribution A,B,C,D
12. Amirav I, Balanov I, Gorenberg M, Groshar D, Luder AS. Nebuliser hood compared to
mask in wheezy infants: aerosol therapy without tears! Archives of Disease in
Childhood, August 2003 88(8); 719-723
IF: 2.616, Rank 16/107 (Pediatrics), Contribution A,B,C,D
13. Jeganathan D, Chodhari R, Meeks M, Faeroe O, Smyth D, Nielsen K, Amirav I, Luder
AS, Bisgaard H, Gardiner RM, Chung EM, Mitchison HM. Loci for primary ciliary
dyskinesia map to 16p 12.1-12.2 and 15q 13.1-15.1 in Faroe islands and Israeli Druze
isolates. Journal of Medical Genetics 2004 41; 233-240
IF: 7.037, Rank 16/156 (Genetics and Heredity), Contribution A,C,D
14. Assy N, Hussein O, Abdallah Khalil, Anthony Luder, Sergio Szvalb, Melia Paizi, and
Gadi Spira. The beneficial effect of aspirin and enoxaparin on fibrosis progression and
regenerative activity in a rat model of cirrhosis. Digestive Diseases and Sciences 2007
May; 52(5):1187-93.
IF: 2.060, Rank 40/71 (Gastroenterology and Hepatology), Contribution A,D
15. A.S. Luder, H. Mandel, M. Khayat, I. Gurevich, P. Frankel, J. Rivlin, Tsippora C. Falik-
Zaccai. Chronic Lung Disease and Cystic Fibrosis Phenotype in Prolidase Deficiency; A
Newly Recognized Association. Journal of Pediatrics 2007;150:656-8
IF: 4.042, Rank 3/107 (Pediatrics), Contribution A,B,C,D
16. Hussein OA, Gefen Y, Zidan JM, Karochero EY, Luder AS, Assy NN, Sror ES, Aviram MY.
LDL oxidation is associated with increased blood hemoglobin A1c levels in diabetic
patients. Clinica Chimica Acta. 2007 Feb; 377(1-2):114-8.
IF: 2.388, Rank 6/30 (Medical Laboratory Technology), Contribution A,D
17. Dov Hershkovitz, Hannah Mandel, Akemi Ishida-Yamamoto, Ilana Chefetz, Bayan
Hino, Anthony Luder, Margarita Indelman, Reuven Bergman, Eli Sprecher. Defective
Lamellar Granule Secretion in Arthrogryposis, Renal dysfunction and Cholestasis
(ARC) syndrome caused by a mutation in VPS33B. Archives of Dermatology 2008
Mar;144(3):334-40
IF: 4.321, Rank 5/54 (Dermatology), Contribution A,B,D
18. AS Luder, SM Tanner, A. de la Chapelle, JH Walter. Amnionless (AMN) Mutations in
Imerslund-Gräsbeck Syndrome May be Associated With Disturbed Vitamin B12
Transport into the CNS. Journal of Inherited Metabolic Disease. 2008 February
31:129;
IF: 3.088, Rank 36/116 (Endocrinology and Metabolism), 46/156 (Genetics and
Heredity) Contribution A,B,C,D
19. Amirav I., Luder AS., Kruger N., Borovitch Y., Babai I., Miron D., Zuker M., Tal G.,
Mandelberg A. A Double-Blind Placebo Controlled Randomised Trial of Montelukast
in Acute Respiratory Syncytial Virus Bronchiolitis. Pediatrics 2008 Dec 122;e1249-
e1255
IF: 5.391, Rank 1/107 (Pediatrics), Contribution B,C,D
20. D. Magen, C. Georgopolous, P. Bross, D. Ang, Y. Segev, A. Nemirovski, E. Shahar, S.
Ravid, A. Luder, B. Heno, R. Gershoni-Baruch, K. Skorecki, H. Mandel. Mitochondrial
Hsp60 Chaperonopathy Causing a Severe Autosomal Recessive Neurodegenerative
Disorder Associated with Brain Hypomyelination and Leukodystrophy. American
Journal of Human Genetics. 2008 83(1):30 – 42
IF: 11.68, Rank 8/156 (Genetics and Heredity), Contribution B,D
21. T. Falik-Zaccai, M. Khyat, A. Luder, P. Savoy, P. Frenkel, Z. Israel, R. Brik, R. Gershoni
Baruch, P. Hechtmann, H. Mandel. A broad spectrum of developmental delay in a
large cohort of prolidase deficiency patients demonstrates marked interfamilial and
intrafamilial phenotypic variability. American Journal of Medical Genetics B
Neuropsychiatr Genet. 2010;153B(1):46-56
IF: 4.156, Rank 23/126 (Psychiatry), Rank 36/156 (Genetics and Heredity)
Contribution A,B,D
22. Newhouse M, Luder A, Chalamish A, Raviv D, Kimmel R, Amirav I. Evidence Based
Design Of Face Masks For Children Using Computerized 3d Face Analysis. Am J Respir
Crit Care Med 2012;185:A5628
23. Israel Amirav, Anthony Luder, Aidah Chleechel, Michael T Newhouse, Miguel
Gorenberg. Lung aerosol deposition in suckling infants. Archives of Disease in
Childhood 2012; 97:497-501
IF: 2.878, Rank 16/106 (Pediatrics), Contribution C,D
24. Israel Amirav, Anthony S. Luder, Asaf Halamish, Dan Raviv, Ron Kimmel, Dan
Waisman, Michael T. Newhouse. Design of aerosol face masks for children using
computerized 3D face analysis. Journal of Aerosol Medicine and Pulmonary Drug
Delivery 2013; 26:1-7
IF: 3.048, Rank 15/50 (Respiratory Medicine), Contribution B,D
25. Israel Amirav, Michael T Newhouse, Anthony Luder, Asaf Halamish, Hamza Omar,
Miguel Gorenberg. Feasibility of aerosol drug delivery to sleeping infants: a
prospective observational study. BMJ Open 2014; 4:e004124 doi:10.1136/bmjopen-
2013-004124
IF: 17.215, Rank 4/154 (General medicine), Contribution A,D
26. Amirav I, Luder AS, Halamish A, Marzuk C, Daitzchman M, Newhouse MT. Computerized
Dead-Space Volume Measurement of Face Masks Applied to Simulated Faces. Respir
Care. 2015 May 5. pii: respcare.03813.
IF: 2.034, Rank 32/54 (Respiratory Medicine)
Clinical Research
1. Luder AS, Holland FJ, Costigan DC, Jenner MR, Wielgosz G, Fazekas AT. Intra-nasal
and sub-cutaneous treatment of central precocious puberty in both sexes with a
long acting analogue of luteinizing hormone-releasing hormone. Journal of Clinical
Endocrinology and Metabolism 1984(Jun); 58(6):966-972
IF: 6.495, Rank 13/116 (Endocrinology and Metabolism), Contribution A,B,C,D
2. Luder AS, Davidson A, Goodman SI, Greene C. Transient non-ketotic hyperglycinemia
in infancy. Journal of Pediatrics 1989(Jun); 114(6):1013-1015
IF: 4.042, Rank 3/107 (Pediatrics), Contribution A,B,C,D
3. Luder AS, Yannicelli S, Greene C. Normal outcome on unrestricted diet after severe
infantile propionic acidemia. Journal of Inherited Metabolic Disease 1989(Dec);
12:307-311
IF: 3.088, Rank 36/116 (Endocrinology and Metabolism), 46/156 (Genetics and
Heredity) Contribution A,B,C,D
4. 4. Davidson-Mundt A, Luder AS, Greene C. Hyperuricemia in medium-chain acyl-
coenzyme A dehydrogenase deficiency. Journal of Pediatrics 1992(Mar);
120(3):444-446
IF: 4.042, Rank 3/107 (Pediatrics), Contribution A,B,C,D
5. Zelnik N, Luder AS, Elpeleg ON, Gross TV, Amir N, Hemli JA, Fattal A, Harel S.
Protracted clinical course for patients with Canavan disease. Developmental
Medicine and Child Neurology 1993(Apr); 35(4):355-358
IF: 3.264, Rank 6/107 (Pediatrics), 52/185 (Clinical Neurology), Contribution A,B,C,D
6. Reis S, Sheffer RN, Merin S, Luder AS, Bach G. Mucolipidosis type IV: a mild form
with late onset. American Journal of Medical Genetics Part A 1993(Sep); 47(3):392-
394
IF: 2.505, Rank 77/156 (Genetics and Heredity), Contribution A,B,C,D
7. Segal-Kuperschmit D, Cozacov C, Luder AS. Idiopathic external hydrocephalus.
Harefuah 1995(Feb); 128(3):150-152
Contribution A,B,C,D
8. Nir-Paz R, Luder AS, Cozacov C, Shahin R. Saphenous neuropathy in adolescence.
Pediatrics 1999(Jan); 103(1):161-163
IF: 5.391, Rank 1/107 (Pediatrics), Contribution A,B,C,D
9. Koren A, Segal-Kupershmit D, Zalman L, Levin C, Abu Hana M, Palmor H, Luder AS,
Attias D. The effect of hydroxyurea in sickle cell anemia; clinical trial in children and
teenagers. Pediatric Hematology Oncology 1999(Jun); 221-232
IF: 0.810, Rank 84/107 (Pediatrics), Contribution A,B,C,D
10. Viner Y, Segal D, Hashkes P, Luder AS. Severe immune hemolysis during ceftriaxone
therapy in Sickle-Cell Anemia Pediatric Infectious Disease Journal 2000 (Jan); 19(1):
83-5
IF: 3.064, Rank 9/107 (Pediatrics), Contribution A,B,C,D
11. Amirav I, Epstien Y, Luder AS. Physiological and practical evaluation of a
biological/chemical protective device for infants. Military Medicine 2000 (Sep)
165(9): 663-6
IF: 0.766, Rank 3/107 (Medicine General and Internal), Contribution B,C,D
12. Luder A. The morbidity and mortality of non-medicine in children. International
Journal of Adolescent Health and Medicine 12; Dec: 2000: 295-306
No longer in print. Contribution B,C,D
13. Dali-Gotfried O, Luder AS. Psychiatric presentation of thyroid disease in
adolescence. International Journal of Adolescent Health and Medicine 12;
Dec:2000: 323-330
No longer in print. Contribution C,D
14. Mandel H, Abeling N, Gutman A, Berant M, Scholten EG, Sheiman C, Luder A, van
Gennip AH. Prolidase deficiency among an Israeli population: prenatal diagnosis in a
genetic disorder with uncertain prognosis. Prenatal Diagnosis 2000; 20:927-929
IF: 2.152, Rank 20/75 (Obstetrics and Gynecology), Contribution A,D
15. Viner Y, Miron D, Yakubov R, Gotfried E, Segal D, Luder A. Neonatal Shigellosis. Israel
Medical Association Journal (IMAJ) 2001(December); 3:964-966
IF: 0.953, Rank 84/151 (Medicine General and Internal), Contribution A,B,C,D
16. Berkovitch M, J. Press, M. Bulkostein, L. Even, J. Barash, R. Brick, D. Tasher, R.
Marom, A.S. Luder, Y. Hecht, M. Rubinstein, M. Mosleh, S. Ben-Shacher, R. Talmor,
A. Zviel, A. Kiro, L. Piglansky, V. Pinsk, Y. Uziel. Pre-Marketing Surveillance of Oral
Ibuprofen Solution in Febrile Children. Clinical Drug Investigation 2001; 21(12):821-
825
IF: 1.622, Rank 167/249 (Pharmacology and Pharmacy), Contribution B,C,D
17. Miron D, Raz R, Luder A. Congenital Toxoplasmosis - The Case for Neonatal
Screening. Israel Medical Association Journal (IMAJ) 2002 (February); 4:119-122
IF: 0.953, Rank 84/151 (Medicine General and Internal), Contribution A,B,D
18. Miron D, Luder A, Horovitz Y, Izkovitz A, Shizgreen I, David EB, Ohnona FS,
Schlesinger Y. Acute human parvovirus B-19 infection in hospitalized children: A
serologic and molecular survey. Pediatric Infectious Disease Journal 2006
Oct;25(10):898-901.
IF: 3.064, Rank 9/107 (Pediatrics), Contribution A,B,C,D
19. I. Amirav, R. Yacobov, AS Luder. Formoterol Turbuhaler Is as Effective as Salbutamol
Diskus in Relieving Adenosine-Induced Bronchoconstriction In Children. Journal of
Aerosol Medicine and Pulmonary Drug Delivery 2007;20:1-6
IF: 2.148, Rank 26/46 (Respiratory System), Contribution A,B,C,D
20. Miron D, Horovitz Y, Luder A, Ohnona FS, Schelisinger Y. Age related IgG
seroprevalence of human Parvovirus B-19 infection in Israeli children. Israel Medical
Association Journal (IMAJ) 2010;12:277-279
IF: 0.953, Rank 84/151 (Medicine General and Internal), Contribution A,B,C,D
21. Butbul-Aviel Y, Mandel H, Avitan-Hersh E, Bergman R, Eshach-Adiv O, Luder A, Brik
R. Prolidase deficiency associated with systemic lupus erythematosus (SLE) : single
site experience and literature review. Pediatric Rheumatology 2012;10:18
IF: 1.79, Rank , Contribution A
22. P. Gilbey, S. Bretler, Y. Avraham, A. Sharabi-Nov, A. Luder. Acupuncture for post-
tonsillectomy pain in children: a randomized, controlled study. Pediatric Anesthesia
2015 Jun;25(6):603-9.
IF: 1.8, Rank, Contribution A,B,C,D
Collaborator:
1. A reach-out system for video microscopy analysis of ciliary motions aiding PCD
diagnosis
Amirav I, Mussaffi H, Roth Y, Schmidts M, Omran H, Werner C. Collaborators Revital
Abitbul, Soliman Alkrinawi, Micha Aviram,Avi Avital, Dorit Baso, Lea Bentur, Hannah
Blau, Malena Cohen-Cymberknoh5, Husein Dabbah, Nael Elias, Arnon Elizur, Shmuel
Goldberg, Avigdor Hevroni,Eytan Kerem, Moran Lavie, Galit Livnat, Anthony Luder,
Avigdor Mandelberg, Michael Paz, Elie Picard, Joseph Rivlin, Moshe Rotschild, David
Shoseyov, Ruth Soferman, Chaim Springer, Johanna Raidt. BMC Research Notes 2015;
8:71
Case Reports
1. Luder AS, Cohen SL, Fisher C. Nephrotic syndrome and renal tubular
dysfunction. Postgraduate Medical Journal 1980(Apr); 56(654):282-287
IF: 1.605, Rank 3/107 (Medicine General and Internal), Contribution A,B,C,D
2. Lorber A, Luder AS. Very early presentation of Pompe's disease and its
cross sectional echocardiographic features. International Journal of
Cardiology 1987(Sep); 16(3):311-314
IF: 6.802, Rank 3/107 (Cardiac & Cardiovascular Systems), Contribution A,B,C,D
3. Lorber A, Luder AS, Dembo L. Acute bacterial endocarditis in early
infancy. International Journal of Cardiology 1987 Dec;17(3):343-5.
IF: 6.802, Rank 3/107 (Cardiac & Cardiovascular Systems), Contribution A,B,C,D
4. Luder AS, Davidson AJ, Goodman SI, Greene CL. Transient non-ketotic
hyperglycinemia in neonates. American Journal of Human Genetics
1988(Sep); 43(3):A13
IF: 11.680, Rank 8/156 (Genetics and Heredity), Contribution A,B,C,D
5. Greene CL, Yannicelli S, Luder AS. Infantile severe propionic acidemia
with normal outcome on unrestricted diet. American Journal of Human
Genetics 1988(Sep); 43(3):A7
IF: 11.680, Rank 8/156 (Genetics and Heredity), Contribution A,B,C,D
6. Luder AS, Naphtali V, Ben-Porat E, Lahat N. Still's disease associated
with adenovirus infection and defect in adenovirus directed natural
killing. Annals of the Rheumatic Diseases 1989; 48:781-786
IF: 9.082, Rank 1/29 (Rheumatology), Contribution A,B,C,D
7. Hardoff R, Luder AS, Lorber A, Dembo L. Early detection of infantile
endocarditis by gallium-67scintigraphy. European Journal of Nuclear
Medicine and Molecular Imaging 1989; 15:219-221
IF: 5.036, Rank 6/111 (Radiology, Nuclear Medicine and Medical Imaging),
Contribution A,B,C,D
8. Segal-Kuperschmit D, Dali-Gotfried O, Luder AS. Water intoxication as a
result of desmopressin overdose. Harefuah 1997; 132:463-465
Contribution B,C,D
9. Luder AS, Segal D, Saba N. Hypoxia and chest pain due to acute
constipation: An under diagnosed condition? Pediatric Pulmonology
1998(Sep); 26(3):222-223
IF: 2.239, Rank 24/107 (Pediatrics), Contribution A,B,C,D
10. Luder AS, Mamet R, Farbstein I, Schoenfeld N. Awareness is the Name of the
Game: Clinical and Biochemical Evaluation of a Case of a Girl Diagnosed With
Acute Intermittent Porphyria Associated With Autism. Cellular and Molecular
Biology 2009(Feb);55:16-19
IF: 0.833, Rank 165/177 (Cell Biology), Contribution A,C,D
11. Gilbey P, Amirav I, Luder A. Vallecular Cyst: A rare cause of failure to thrive
without respiratory distress in an infant The Journal of Pediatrics June 2011
(eprint)
IF: 4.042, Rank 3/107 (Pediatrics), Contribution A,B,C,D
12. Gilbey P, Bretler S, Even-Tov E, Luder A. Accidental out-of-hospital delivery
complicated by acute neonatal parotitis: Case report and a review of the
literature. International Journal of Pediatric Otorhinolaryngology Extra 2011
DOI:10.1016/j.pedex.2011.05.001
IF: 1.067, Rank 67/107 (Pediatrics) 21/41 (Otorhinolaryngology), Contribution
B,C,D
Reviews
1. Luder A, Klein O, Gotfried O, Eshel B, Carbohydrate-deficient Glycoprotein
Syndromes - A New Group of Multi-System Genetic Disorders. Harefuah
1999(Nov 15); 137(10):486-490
Contribution A,B,C,D
2. Dali-Gotfried O, Viner Y Luder AS. The controversy surrounding Paracetomol
therapy in childhood. Harefuah 2000;138: 997-1000
Contribution A,B,C,D
3. Viner Y, Dali-Gotfrid O, Luder A, Hashkes P. Ibuprofen – new era of an old drug.
Harefuah; 140(9); Sep:2001: 868-871
Contribution A, B,C,D
4. Luder AS. Complementary and alternative medicine. Israel Medical Association
Journal (IMAJ). 2004 Apr;6(4):255-6.
IF: 0.953, Rank 84/151 (Medicine General and Internal), Contribution A,B,C,D
5. Amirav I, Luder A, Viner Y, Finkel M. Decriminalization of Cannabis – potential
risks for children? Acta Paediatrica 2010;100:618-620
IF: 1.955, Rank 33/107 (Pediatrics), Contribution B,C,D
Invited Editorials
1. Evidence-Based Clinical Practice Guidelines – What is the Evidence? Israel Medical
Association Journal (IMAJ) 2011;13:689-691
IF: 0.953, Rank 84/151 (Medicine General and Internal), Contribution A,B,C,D
Letters
1. A.S. Luder. Alternative forms of medicine (letter). Israel Medical Association
Journal (IMAJ) 2007;9:494
IF: 0.953, Rank 84/151 (Medicine General and Internal), Contribution A,B,C,D
Books
1. Subcutaneous and intra-nasal D-Ser (TBU)6-LHRH (Buserilin) in the
management of precocious puberty. Holland FJ, Fishman L, Luder AS,
Costigan DC, Jenner M, Wielgosz G, Fazekas A. Proceedings of the 7th
International Congress of Endocrinology, 1985, Elsevier Science
Publishers.
2. Israel Encyclopedia of Health 2003
1. Chapter on “Congenital Disorders of Glycosylation”
2. Chapter on “ Fraternal Twins”
3. Guidelines for the Diagnosis and Treatment of Acute Otitis Media. Spenser T.,
Miron D., Zohar S, Persiko M, Luder A. Joint Working Party of Kupat Holim Clalit
and Faculty of Medicine, Technion. Printings 2001 (twice), 2003
4. Chapters on: 1. Phenylketonuria 2. Syndromes in Paediatrics (Ministry of Health
Handbook for "Tipat Halav" Mother and Infant Clinics, והפעות התינוק בריאות
Dionon, Tel Aviv, 2011 pp 99-103, 107-110
Non-peer Reviewed Papers
1. Luder AS. Recent trends in the relationship between medicine and medical
marketing forces. International Journal of Medical Marketing; 2005 (April)
5(2):172-174
Contribution A,B,C,D
2. A. Luder. The 10th International Congress of Inborn Errors of Metabolism (ICIEM)
Makahuri Messe (Tokyo), Japan, September 2006. Pediatric Endocrinology
Reviews 2007 March;4(3):235-236
Contribution B,C,D
3. AS Luder. Immunizations in Israel-Present and Future Problems (Hebrew). Israel
Journal of Pediatrics 2007 December 62:9-12
Contribution A,B,C,D
4. Luder AS. RSV Bronchioloitis-Present and Future. Medical 2009; 25:61-63
Contribution A,B,C,D
5. Anthony Luder. Israel Society for Metabolic Diseases, Winter Meeting, Hadassah
Medical Centre , Ein Kerem, Jerusalem, Israel (December 7, 2011) Pediatric
Endocrinology Reviews (PER) Q Volume 9 Q No. 2 Q December 2011.
Contribution B,C,D
Citation Statistics
Total number of citations (Web of Science ISI Web of Knowledge): 707 (07-11)
4 most cited papers:
Parker WD, Boyson SJ, Luder AS, Parks J. Evidence for a defect in NADH:ubiquinone
oxidoreductase (complex I) in Huntington's disease. Neurology 1990;40:1231-1233 Citations
188
Luder AS, Holland FJ, Costigan DC, Jenner MR, Wielgosz G, Fazekas AT. Intra-nasal and sub-
cutaneous treatment of central precocious puberty in both sexes with a long acting analogue
of luteinizing hormone-releasing hormone. Journal of Clinical Endocrinology and
Metabolism 1984;58:966-972 Citations 76
Barbara Schenk, Timo Imbach, Christian G. Frank, Claudia E. Grubenmann, Gerald V.
Raymond, H. Hurvitz, A. Raas-Rotschild, Anthony S. Luder, Jaak Jaeken, Eric G. Berger, Gert
Matthijs, Thierry Hennet and Markus Aebi. MPDU1 mutations underlie a novel human
congenital disorder of glycosylation, designated type If. Journal of Clinical Investigation
2001;108:1687-1695 Citations 51
Shatzky S, Moses S, Levy J, Pinsk V, Hershkovitz E, Herzog L, Shorer Z, Luder A, Parvari R.
Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic
heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results
of nerve conduction studies. American Journal of Medical Genetics 2000;92:353-60
Citations 43
Conferences
A. Plenary - Invited talks
Conference Place and Date Title of Lecture/Poster
Society for Pediatric Research
1982, Washington DC., USA. A new LHRH analogue, D-Ser
(TBU)6-LHRH 1-9 EA10 (HOE
766) in central precocious
puberty: subcutaneous and
intra-nasal therapy in 6 girls
and 1 boy. (Pediatric Research
1983(Apr);17(4,2):166A. )
Israel Association for Pediatric
Neurology
1989, Jerusalem Therapeutic and toxic
mechanisms of Valproic Acid
Annul Harvey Levitt Symposium
on Inherited Disorders of
Metabolism
1990, Technion, Haifa Inherited Disorders of β-
oxidation of fats
6th International Congress of
Child Development Centers
1991 Nazareth Molecular genetics and
mental retardation
Israel Society for Metabolic
Disease
1998, Tel-Aviv Carbohydrate-deficient
glycoprotein syndromes
(Congenital Disorders of
Glycosylation CDG)
Israel Clinical Pediatrics Society 2000, Tel Aviv Infantile botulism
Israel Society for Metabolic
Disease, Ann Rappaport
Symposium on
Aminoacidopathies and
Development
2002, Faculty of Medicine, Technion,
Haifa
Cystic Fibrosis and Prolidase
deficiency
Annual Conference on Paediatric
Updates, Clalit Health Services
2009, Tiberius Recent developments in the
genetics of congenital heart
disease
Israel Medical Association
International Forum Conference
2009, Tel Aviv Progress, pre-natal selection
and the ethical consumer
Association of Clinical Research
Professionals (ACRP) 5th Annual
Conference
2010, Airport City Research ethics and
regulatory committees-future
perspectives
1st National Conference Israel
Branch of Orphanet International
2011, Schneider Children’s Hospital,
Petah Tiqwa
Orphan drugs – Who wishes
to adopt them?
National course on neurological
aspects inherited metabolic
2011, Asaf Harofe Hospital Metabolic investigation of
acute neurological disease in
disease childhood
International Society for
Pharmacoeconomics and
Outcomes Research ISPOR 4th
Annual Congress
2011, Herzliya Orphan diseases and orphan
drugs
Association of Pharmacists in
Israel, Ministry of Health
2011, Eilat Orphan diseases and orphan
drugs
B. Oral Presentations and Posters
Conference Place, Date, Speaker (presenter) Title of Lecture/Poster
Society for Inherited Metabolic
Disease SIMD
1988 Asilomar, California, USA.
A.S.Luder
Transient non-ketotic
hyperglycinemia in neonates
American Society of Human
Genetics
1988 New Orleans, Louisiana, USA.
A.S.Luder
Infantile severe propionic
acidemia
Israel Society for Human
Genetics
1989 Jerusalem
A.S.Luder
1. Kinetically abnormal
lipoamide
dehydrogenase and
lactic acidosis
2. Use of platelets in the
investigation of
mitochondrial
metabolism
Society for Inherited Metabolic
Disease SIMD
1989 Orlando, Florida, USA.
A.S.Luder
1. Inactivation of alpha-
ketoglutarate
dehydrogenase by
valproic acid (Prize for
Best Fellow Research)
2. Vertical transmission
of lactic acidosis;
phenotypes and
genetic implications
10th David Smith Meeting on
Birth Defects and Morphogenesis
1989 Madrid, Spain
Prof. C. Greene
Lactic acidosis and Williams
phenotype. (Published in
Haywood Journal of
Dysmorphology)
American Association of
Neurology
1990 Miami, Florida
A.S.Luder
Complex I abnormalities in
Huntington disease
Society for Inherited Metabolic
Disease, SIMD
1991 Santa Fe, New Mexico, USA
A.S.Luder
Bicycle ergometry in complex
I deficiency
Society for the Study of Inherited 1994 Manchester, UK. Fanconi syndrome, diabetes,
Errors of Metabolism SSIEM A.S.Luder complex I deficiency and
mtDNA deletion
Israel Association for Clinical
Paediatrics
1995 Tel-Aviv
A.S.Luder
Risk factors in unexplained
irritability in infancy
Israel Haematology and Oncology
Association
2002 Tel-Aviv
A.S.Luder
Long-term use of hydroxyurea
and follow-up in the
management of Sickle-Cell
anaemia and Sickle-
thalassemia
2nd International Congress on
Paediatrics in the Community
2000 Jerusalem
A.S.Luder
1. The morbidity and
mortality of non-
medical treatment of
children
2. Consensus guidelines
for the diagnosis and
treatment of acute
otitis media in
children
“Europaediatrics 2000” (Union of
National European Paediatric
Societies, Confederation of
European Specialists in
Paediatrics)
2000 Rome, Italy
A.S.Luder
1. Epidemiology and risk
factors for
unexplained extreme
irritability in infancy
2. Studies in the
Imerslund-Gräsbeck
syndrome, evidence
for a blood-brain
barrier for vitamin
B12
4th International Congress of
Paediatric Pulmonology
2000 Nice, France
Prof. I. Amirav
The use of a hood interface
for the delivery of nebulised
drugs in infancy. Winner of
International Prize for
Outstanding Research).
12th Congress European Society
for Paediatric Infectious Disease
ESPID
2001 Istanbul, Turkey
Prof. D. Miron
Neonatal Shigellosis
Society for the Study of Inborn
Errors of Metabolism SSIEM
2001 Prague, Czech Republic
A.S.Luder
Dominant Inheritance of
Complex IV Deficiency with
Psychiatric Presentation
9th International Congress on
Metabolism ICM
2003 Brisbane, Australia
A.S.Luder
Oral presentation: Prolidase
deficiency and chronic lung
disease in childhood.
Prolidase deficiency causes
chronic lung disease and CF.
Journal of Inherited Metabolic
Disease; 2003 (September)
26(Supplement 2): 67
Meeting on Lipid Metabolism 2004 Technion, Haifa
Dr. H. Osama
The contribution of LDL
Tendency to Peroxidation to
Plasma Hemoglobin A1C Level
in Diabetic Patients
European Society for Paediatric
Infectious Disease ESPID
2005 Valencia, Spain
A.S.Luder
Megadose methylprednisone
treatment of acute retinal
necrosis due to Varicella with
good prognosis
10th International Congress on
Inborn Errors of Metabolism ICM
2006 Makuhari, Chiba-Tokyo, Japan
A.S.Luder
1. Citrullinemia type II
outside east Asia-the
Israeli experience
2. Acute intermittent
porphyria presenting
as pervasive
developmental
disorder and mental
retardation
17th World Congress on Medicine
and Law
2008 Beijing, China
A.S.Luder
Ethical and legal dilemmas
regarding immunisation
programmes
European Society for Congenital
Disorders of Metabolism
2008 Amsterdam, Holland
Prof. H. Mandel
Fructose intolerance mimics
CDG I
Genome Stability in Health and
Disease. Institute for Advanced
Studies
2008 Hebrew University Jerusalem
Dr. Z. Falik-Borenstein
A common mutation in the
CSB gene is responsible for
the severe type II Cockayne
syndrome among Druze in
northern Israel
National Conference on Nature,
Nurture and Research in Autism-
Combined Challenges
2009 Sheba Medical Centre, Tel
Hashomer
A.S.Luder
Acute Intermittent Porphyria
Associated with Pervasive
Developmental Disorder
International Congress on
Bioethics Committees in
Hospitals
2009 Safed (under auspices of UNESCO
and International Centre for Law Ethics
and Medicine, University of Haifa)
A.S.Luder
Current regulatory
atmosphere may be harming
clinical research. An ethical
paradox
81st Berzelius Symposium on
Porphyrias
2009 Swedish Society of Medicine,
Stockholm, Sweden
A.S.Luder
Awareness is the Name of the
Game; Autism and Acute
Porphyria
European Society of Paediatric
Infectious Diseases ESPID
2010 Nice, France
A.S.Luder
Acute B cell lymphoblastic
leukaemia presenting as non-
tropical pyomyositis due to
Streptococcus G in a 6-year-
old girl
3rd Annual Wingate Conference
on the Advancement and
Development of Sport in Israel
2010 Jerusalem
Prof. Y. Weinstein
Recovery of muscle power
following 30s Wingate Arms
Anaerobic Test: Comparing
boys and men
Israel Association Medical
Genetics
2010 Jerusalem National registry for Primary
Ciliary Dyskinesia
Israel Society for Otolaryngology
and Head and Neck Surgery
2011 Eilat 1. An Accidental Out-Of-
Hospital Delivery
Complicated by Acute
Neonatal Parotitis
2. Histiocytic Necrotizing
(Kickuchi)
Lympadenitis
18th International Congress for
Aerosols in Medicine
2011 Rotterdam, Holland Lung Aerosol Deposition in
Suckling Infants
Experimental Biology 2013 Boston, USA Building a new anatomy
program in Israel
5th International Clinical Skills
Conference
2013 Prato, Italy
A. S. Luder
1. An Innovative clinical skills
program in a new medical
school
2. Establishing a Mentorship
Program in a New Medical
School
Other Major Conference Participation
7th International Congress on Inherited Disorders of
Metabolism
1997, Vienna, Austria
3rd International Conference on Urea Cycle Disorders 1997, Vienna, Austria
Course on Carbohydrate Deficient Glycoprotein
Syndrome
1997 University of Amsterdam, Holland
8th Annual Conference American College of Medical
Genetics
1999 Miami, FL, USA
8th International Congress on Inherited Disorders of
Metabolism
2000 Cambridge, UK
European Haematology and Oncology Association Bi-
national Congress
2002 Paris, France
2nd International Congress on Chronic Disorders in
Childhood (Session Chairman)
2008 Jerusalem
10th International Workshop on Lysosomal Storage
Disorders
2010 Prague, Czech Republic
10th International Symposium on Lysosomal Storage
Disease
2011 Madrid, Spain
11th International Workshop on Lysosomal Storage
Disorders
2012 London, UK
Society for the Study of Inborn Errors of Metabolism
Annual Meeting
2012 Birmingham, UK
Society for the Study of Inborn Errors of Metabolism
Annual Meeting
2014 Innsbruck Austria
C. Participation in Organizing Conferences and Courses
Conference Place and Time Role
Israel Metabolic Society summer
conference-Storage disease
Soroka Medical Centre, Beer Sheva,
July 2013
Head of society and organizing
committee
Israel Metabolic Society winter
conference-Neuro-metabolic
disease
Wolfson Medical Centre, Bat Yam,
Israel, February 2013
Head of society and organizing
committee
Israel Metabolic Society winter
conference-Diagnostic methods
Hadassah Medical Centre, Ein
Kerem, Jerusalem, December 2011
Head of society and organizing
committee
Israel Metabolic Society-New
Developments in Neurometabolic
Disease
Ha-Emek Medical Centre, Afula,
June 6 2011 Head of society and organizing
committee
3rd Ziv International Conference in
the Galilee-Advances in Trauma
and Trauma Orthpaedics.
Attendance 105 physicians. Budget
NIS 97,000. Academic aegis: Bar
Ilan Faculty of Medicine; Technion
Faculty of Medicine; Israel
Kfar Giladi, May 12-14 2011 Member of organizing committee
Association of Orthopaedics; Israel
Association of Plastic and Aesthetic
Surgery; Israel Medical Association
Israel Metabolic Society-Neonatal
Screening in Israel
Dana Children’s Hospital-Ichilov,
Tel Aviv, March 12, 2011 Head of society and organizing
committee
2nd Ziv International Conference in
the Galilee-Advances in
Hepatology. (In collaboration with
University of Lille, France and
Scientific Attaché Embassy of
France in Israel). Attendance 105
physicians. Budget NIS 67,000.
Academic aegis Technion Faculty of
Medicine; Israel Association of
Hepatology; Israel Paediatric
Association; Israel Medical
Association
Ramot, Golan, May 2010 Director organizing committee
1st Ziv International Conference in
the Galilee- Modern Paediatric
Anaesthesia (in collaboration with
University of Lille, France and
Scientific Attaché Embassy of
France in Israel). Attendance 87
physicians. Budget NIS 25,000.
Academic aegis; Technion faculty
of Medicine; Israel Association of
Anaesthetists; Israel Paediatric
Association; Israel Medical
Association
Hagoshrim, April 2009 Initiator and head of organizing
committee
1st National Course for First Part of
Specialty Examination in
Paediatrics (on behalf of the Israel
Association for Paediatricians).
Attendance 96 residents. Budget
65,000 NIS. 28 hours of instruction,
faculty 18 lecturers.
Zichron Yaakov, May 2008 Director and sole organizer
Israel Metabolic Society-Early
Detection of Metabolic Disease
Rambam Hospital, September 2007 Member of organizing committee
International Meeting on Ayelet Hashachar, July 2003 Director of organizing committee
Paediatric Lung Disease and
Empyema
Medical License Course for new
physician immigrants from East
Europe and South America (46
students, 560 hours instruction)
Academic aegis: Faculty of
Medicine (Technion) and the
Ministries of Health and Immigrant
Absorbtion. Success rate in
national licensing exams 55% on
first attempt (national average
22%).
Ziv Medical Centre, 2002 Director and organiser
National Conference on Paediatrics Safed, 2002 Director of organizing committee