Gross-Tsur V - Search Results

1

Gaucher's disease variant characterised by progressive calcification of heart valves and unique genotype.

Abrahamov A, Elstein D, Gross-Tsur V, Farber B, Glaser Y, Hadas-Halpern I, Ronen S, Tafakjdi M, Horowitz M, Zimran A. Abrahamov A, et al. Lancet. 1995 Oct 14;346(8981):1000-3. doi: 10.1016/s0140-6736(95)91688-1. Lancet. 1995. PMID: 7475546

2

Oculomotor apraxia: the presenting sign of Gaucher disease.

Gross-Tsur V, Har-Even Y, Gutman I, Amir N. Gross-Tsur V, et al. Pediatr Neurol. 1989 Mar-Apr;5(2):128-9. doi: 10.1016/0887-8994(89)90042-8. Pediatr Neurol. 1989. PMID: 2712947

3

Anthropometric adjustments are helpful in the interpretation of BMD and BMC Z-scores of pediatric patients with Prader-Willi syndrome.

Hangartner TN, Short DF, Eldar-Geva T, Hirsch HJ, Tiomkin M, Zimran A, Gross-Tsur V. Hangartner TN, et al. Osteoporos Int. 2016 Dec;27(12):3457-3464. doi: 10.1007/s00198-016-3671-y. Epub 2016 Jul 4. Osteoporos Int. 2016. PMID: 27377921

4

Unique congenital features in tuberous sclerosis.

Gross-Tsur V, Klar A, Gazit D, Shalev RS. Gross-Tsur V, et al. Clin Pediatr (Phila). 1992 Jun;31(6):364-5. doi: 10.1177/000992289203100610. Clin Pediatr (Phila). 1992. PMID: 1628471 No abstract available.

5

Developmental dyscalculia and brain laterality.

Shalev RS, Manor O, Amir N, Wertman-Elad R, Gross-Tsur V. Shalev RS, et al. Cortex. 1995 Jun;31(2):357-65. doi: 10.1016/s0010-9452(13)80368-1. Cortex. 1995. PMID: 7555012

6

Familial microcephaly with severe neurological deficits: a description of five affected siblings.

Gross-Tsur V, Joseph A, Blinder G, Amir N. Gross-Tsur V, et al. Clin Genet. 1995 Jan;47(1):33-7. doi: 10.1111/j.1399-0004.1995.tb03918.x. Clin Genet. 1995. PMID: 7774041

7

Developmental right-hemisphere syndrome: clinical spectrum of the nonverbal learning disability.

Gross-Tsur V, Shalev RS, Manor O, Amir N. Gross-Tsur V, et al. J Learn Disabil. 1995 Feb;28(2):80-6. J Learn Disabil. 1995. PMID: 7884301

8

Developmental dyscalculia is a familial learning disability.

Shalev RS, Manor O, Kerem B, Ayali M, Badichi N, Friedlander Y, Gross-Tsur V. Shalev RS, et al. J Learn Disabil. 2001 Jan-Feb;34(1):59-65. doi: 10.1177/002221940103400105. J Learn Disabil. 2001. PMID: 15497272

9

Factors influencing diagnosis delay in children with Tourette syndrome.

Shilon Y, Pollak Y, Benarroch F, Gross-Tsur V. Shilon Y, et al. Eur J Paediatr Neurol. 2008 Sep;12(5):398-400. doi: 10.1016/j.ejpn.2007.10.006. Epub 2007 Dec 4. Eur J Paediatr Neurol. 2008. PMID: 18055232

10

Primary ovarian dysfunction contributes to the hypogonadism in women with Prader-Willi Syndrome.

Eldar-Geva T, Hirsch HJ, Rabinowitz R, Benarroch F, Rubinstein O, Gross-Tsur V. Eldar-Geva T, et al. Horm Res. 2009;72(3):153-9. doi: 10.1159/000232489. Epub 2009 Sep 1. Horm Res. 2009. PMID: 19729946

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