Weintrob N - Search Results

1

Adult height of subjects with nonclassical 21-hydroxylase deficiency.

Eyal O, Tenenbaum-Rakover Y, Shalitin S, Israel S, Weintrob N. Eyal O, et al. Among authors: weintrob n. Acta Paediatr. 2013 Apr;102(4):419-23. doi: 10.1111/apa.12147. Epub 2013 Jan 28. Acta Paediatr. 2013. PMID: 23298233

2

Non-classical 21-hydroxylase deficiency in infancy and childhood: the effect of time of initiation of therapy on puberty and final height.

Weintrob N, Dickerman Z, Sprecher E, Galatzer A, Pertzelan A. Weintrob N, et al. Eur J Endocrinol. 1997 Feb;136(2):188-95. doi: 10.1530/eje.0.1360188. Eur J Endocrinol. 1997. PMID: 9116914

3

HLA class II immunogenetics of IDDM in Yemenite Jews.

Israel S, Kwon OJ, Weintrob N, Sprecher E, Bloch K, Assa S, Brautbar C, Vardi P. Israel S, et al. Among authors: weintrob n. Hum Immunol. 1998 Nov;59(11):728-33. doi: 10.1016/s0198-8859(98)00074-3. Hum Immunol. 1998. PMID: 9796741

4

Neonatal pig islets induce a lower T-cell response than adult pig islets in IDDM patients.

Bloch K, Assa S, Lazard D, Abramov N, Shalitin S, Weintrob N, Josefsberg Z, Rapoport M, Vardi P. Bloch K, et al. Among authors: weintrob n. Transplantation. 1999 Mar 15;67(5):748-52. doi: 10.1097/00007890-199903150-00018. Transplantation. 1999. PMID: 10096533

5

Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency.

Weintrob N, Brautbar C, Pertzelan A, Josefsberg Z, Dickerman Z, Kauschansky A, Lilos P, Peled D, Phillip M, Israel S. Weintrob N, et al. Eur J Endocrinol. 2000 Sep;143(3):397-403. doi: 10.1530/eje.0.1430397. Eur J Endocrinol. 2000. PMID: 11022183

6

Type 1 diabetes environmental factors and correspondence analysis of HLA class II genes in the Yemenite Jewish community in Israel.

Weintrob N, Sprecher E, Israel S, Pinhas-Hamiel O, Kwon OJ, Bloch K, Abramov N, Arbel A, Josefsberg Z, Brautbar C, Vardi P. Weintrob N, et al. Diabetes Care. 2001 Apr;24(4):650-3. doi: 10.2337/diacare.24.4.650. Diabetes Care. 2001. PMID: 11315825

7

Bedside scoring procedure for the diagnosis of diabetic peripheral neuropathy in young patients with type 1 diabetes mellitus.

Shalitin S, Josefsberg Z, Lilos P, de-Vries L, Phillip M, Weintrob N. Shalitin S, et al. Among authors: weintrob n. J Pediatr Endocrinol Metab. 2002 May;15(5):613-20. doi: 10.1515/jpem.2002.15.5.613. J Pediatr Endocrinol Metab. 2002. PMID: 12014520

8

Adrenal hypoplasia congenita with multiple pituitary hormone deficiency without documented mutation in DAX1 or SF1 gene.

Shalitin S, Josefsberg Z, Vilain E, Shomrat R, Weintrob N. Shalitin S, et al. Among authors: weintrob n. Mol Genet Metab. 2002 Jun;76(2):157-61. doi: 10.1016/s1096-7192(02)00029-x. Mol Genet Metab. 2002. PMID: 12083815

9

Decreased cortisol secretion in nonclassical 21-hydroxylase deficiency before and during glucocorticoid therapy.

Weintrob N, Israel S, Lazar L, Lilos P, Brautbar C, Phillip M, Pertzelan A. Weintrob N, et al. J Pediatr Endocrinol Metab. 2002 Jul-Aug;15(7):985-91. doi: 10.1515/jpem.2002.15.7.985. J Pediatr Endocrinol Metab. 2002. PMID: 12199343

10

Comparison of continuous subcutaneous insulin infusion and multiple daily injection regimens in children with type 1 diabetes: a randomized open crossover trial.

Weintrob N, Benzaquen H, Galatzer A, Shalitin S, Lazar L, Fayman G, Lilos P, Dickerman Z, Phillip M. Weintrob N, et al. Pediatrics. 2003 Sep;112(3 Pt 1):559-64. doi: 10.1542/peds.112.3.559. Pediatrics. 2003. PMID: 12949284 Clinical Trial.

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