Laron Z - Search Results

1

The E180splice mutation in the GHR gene causing Laron syndrome: witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?

Gonçalves FT, Fridman C, Pinto EM, Guevara-Aguirre J, Shevah O, Rosembloom AL, Hwa V, Cassorla F, Rosenfeld RG, Lins TS, Damiani D, Arnhold IJ, Laron Z, Jorge AA. Gonçalves FT, et al. Among authors: laron z. Am J Med Genet A. 2014 May;164A(5):1204-8. doi: 10.1002/ajmg.a.36444. Epub 2014 Mar 24. Am J Med Genet A. 2014. PMID: 24664892

2

Genetic analysis of the pedigrees and molecular defects of the GH-receptor gene in the Israeli cohort of patients with Laron syndrome.

Shevah O, Laron Z. Shevah O, et al. Among authors: laron z. Pediatr Endocrinol Rev. 2006 Aug;3 Suppl 3:489-97. Pediatr Endocrinol Rev. 2006. PMID: 17551471

3

Molecular defects of the growth hormone receptor gene, including a new mutation, in Laron syndrome patients in Israel: relationship between defects and ethnic groups.

Shevah O, Rubinstein M, Laron Z. Shevah O, et al. Among authors: laron z. Isr Med Assoc J. 2004 Oct;6(10):630-3. Isr Med Assoc J. 2004. PMID: 15473594 Free article.

4

Classical phenotype of Laron syndrome in a girl with a heterozygous mutation and heterozygous polymorphism of the growth hormone receptor gene.

Shevah O, Galli-Tsinopoulou A, Rubinstein M, Nousia-Arvanitakis S, Laron Z. Shevah O, et al. Among authors: laron z. J Pediatr Endocrinol Metab. 2004 Mar;17(3):371-4. doi: 10.1515/jpem.2004.17.3.371. J Pediatr Endocrinol Metab. 2004. PMID: 15112915

5

The intellectual capacity of patients with Laron syndrome (LS) differs with various molecular defects of the growth hormone receptor gene. Correlation with CNS abnormalities.

Shevah O, Kornreich L, Galatzer A, Laron Z. Shevah O, et al. Among authors: laron z. Horm Metab Res. 2005 Dec;37(12):757-60. doi: 10.1055/s-2005-921097. Horm Metab Res. 2005. PMID: 16372230 Clinical Trial.

6

Intronic mutation in the growth hormone receptor gene in a Peruvian girl with Laron syndrome.

Shevah O, Nunez O, Rubinstein M, Laron Z. Shevah O, et al. Among authors: laron z. J Pediatr Endocrinol Metab. 2002 Jul-Aug;15(7):1039-40. doi: 10.1515/jpem.2002.15.7.1039. J Pediatr Endocrinol Metab. 2002. PMID: 12199333 No abstract available.

7

Receptor mutations and haplotypes in growth hormone receptor deficiency: a global survey and identification of the Ecuadorean E180splice mutation in an oriental Jewish patient.

Berg MA, Peoples R, Pérez-Jurado L, Guevara-Aguirre J, Rosenbloom AL, Laron Z, Milner RD, Francke U. Berg MA, et al. Among authors: laron z. Acta Paediatr Suppl. 1994 Apr;399:112-4. doi: 10.1111/j.1651-2227.1994.tb13302.x. Acta Paediatr Suppl. 1994. PMID: 7949594

8

Congenital IGF1 deficiency tends to confer protection against post-natal development of malignancies.

Steuerman R, Shevah O, Laron Z. Steuerman R, et al. Among authors: laron z. Eur J Endocrinol. 2011 Apr;164(4):485-9. doi: 10.1530/EJE-10-0859. Epub 2011 Feb 3. Eur J Endocrinol. 2011. PMID: 21292919

9

Identification of two novel mutations in the human growth hormone receptor gene.

Shevah O, Borrelli P, Rubinstein M, Laron Z. Shevah O, et al. Among authors: laron z. J Endocrinol Invest. 2003 Jul;26(7):604-8. doi: 10.1007/BF03347015. J Endocrinol Invest. 2003. PMID: 14594108

10

Laron syndrome. First report from Greece.

Galli-Tsinopoulou A, Nousia-Arvanitakis S, Tsinopoulos I, Bechlivanides C, Shevah O, Laron Z. Galli-Tsinopoulou A, et al. Among authors: laron z. Hormones (Athens). 2003 Apr-Jun;2(2):120-4. doi: 10.14310/horm.2002.1191. Hormones (Athens). 2003. PMID: 17003011 Free article.

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