Halac I - Search Results

1

Endocrine manifestations of craniopharyngioma.

Halac I, Zimmerman D. Halac I, et al. Childs Nerv Syst. 2005 Aug;21(8-9):640-8. doi: 10.1007/s00381-005-1246-x. Epub 2005 Jul 27. Childs Nerv Syst. 2005. PMID: 16047216 Review.

2

Evaluating short stature in children.

Halac I, Zimmerman D. Halac I, et al. Pediatr Ann. 2004 Mar;33(3):170-6. doi: 10.3928/0090-4481-20040301-08. Pediatr Ann. 2004. PMID: 15054931 Review.

3

Managing growth hormone treatment in pediatric patients.

Halac I, Zimmerman D. Halac I, et al. Pediatr Ann. 2004 Mar;33(3):183-8. doi: 10.3928/0090-4481-20040301-10. Pediatr Ann. 2004. PMID: 15054933 Review.

4

Coordinating care for children with Turner syndrome.

Halac I, Zimmerman D. Halac I, et al. Pediatr Ann. 2004 Mar;33(3):189-96. doi: 10.3928/0090-4481-20040301-11. Pediatr Ann. 2004. PMID: 15054934 Review.

5

Thyroid nodules and cancers in children.

Halac I, Zimmerman D. Halac I, et al. Endocrinol Metab Clin North Am. 2005 Sep;34(3):725-44, x. doi: 10.1016/j.ecl.2005.04.007. Endocrinol Metab Clin North Am. 2005. PMID: 16085168 Review.

6

Central and gonadal hypogonadism in X-linked lissencephaly.

Halac I, Habiby R, Curran J, Zimmerman D. Halac I, et al. J Pediatr Endocrinol Metab. 2006 Jul;19(7):955-7. doi: 10.1515/jpem.2006.19.7.955. J Pediatr Endocrinol Metab. 2006. PMID: 16995578

7

Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor.

Ali A, Christie PT, Grigorieva IV, Harding B, Van Esch H, Ahmed SF, Bitner-Glindzicz M, Blind E, Bloch C, Christin P, Clayton P, Gecz J, Gilbert-Dussardier B, Guillen-Navarro E, Hackett A, Halac I, Hendy GN, Lalloo F, Mache CJ, Mughal Z, Ong AC, Rinat C, Shaw N, Smithson SF, Tolmie J, Weill J, Nesbit MA, Thakker RV. Ali A, et al. Among authors: halac i. Hum Mol Genet. 2007 Feb 1;16(3):265-75. doi: 10.1093/hmg/ddl454. Epub 2007 Jan 8. Hum Mol Genet. 2007. PMID: 17210674

8

An integrated strategy for the diagnosis of neuronal ceroid lipofuscinosis types 1 (CLN1) and 2 (CLN2) in eleven Latin American patients.

Kohan R, Cismondi IA, Kremer RD, Muller VJ, Guelbert N, Anzolini VT, Fietz MJ, Ramírez AM, Halac IN. Kohan R, et al. Among authors: halac in. Clin Genet. 2009 Oct;76(4):372-82. doi: 10.1111/j.1399-0004.2009.01214.x. Clin Genet. 2009. PMID: 19793312

9

Gene symbol: CLN6. Disease: Neuronal ceroid lipofuscinosis, late Infantile.

Cismondi IA, Kohan R, Ghio A, Ramirez AM, Halac IN. Cismondi IA, et al. Among authors: halac in. Hum Genet. 2008 Oct;124(3):324. Hum Genet. 2008. PMID: 18846690 No abstract available.

10

Gene symbol: CLN6. Disease: Neuronal ceroid lipofuscinosis, late infantile.

Cismondi IA, Kohan R, Ghio A, Ramirez AM, Halac IN. Cismondi IA, et al. Among authors: halac in. Hum Genet. 2008 Oct;124(3):323-4. Hum Genet. 2008. PMID: 18846689 No abstract available.

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