Keselman A - Search Results

1

SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity.

Binder G, Renz A, Martinez A, Keselman A, Hesse V, Riedl SW, Häusler G, Fricke-Otto S, Frisch H, Heinrich JJ, Ranke MB. Binder G, et al. Among authors: keselman a. J Clin Endocrinol Metab. 2004 Sep;89(9):4403-8. doi: 10.1210/jc.2004-0591. J Clin Endocrinol Metab. 2004. PMID: 15356038

2

Growth in small for gestational age children. Growth hormone therapy.

Keselman A. Keselman A. Arch Argent Pediatr. 2023 Aug 1;121(4):e202202967. doi: 10.5546/aap.2022-02967.eng. Epub 2023 Mar 2. Arch Argent Pediatr. 2023. PMID: 36728710 Free article. English, Spanish. No abstract available.

3

Case report: Novel SIN3A loss-of-function variant as causative for hypogonadotropic hypogonadism in Witteveen-Kolk syndrome.

Correa Brito L, Keselman A, Villegas F, Scaglia P, Esnaola Azcoiti M, Castro S, Sanguineti N, Izquierdo A, Maier M, Bergadá I, Arberas C, Rey RA, Ropelato MG. Correa Brito L, et al. Among authors: keselman a. Front Genet. 2024 Mar 11;15:1354715. doi: 10.3389/fgene.2024.1354715. eCollection 2024. Front Genet. 2024. PMID: 38528912 Free PMC article.

4

Diagnosing and treating anterior pituitary hormone deficiency in pediatric patients.

Rey RA, Bergadá I, Ballerini MG, Braslavsky D, Chiesa A, Freire A, Grinspon RP, Keselman A, Arcari A. Rey RA, et al. Among authors: keselman a. Rev Endocr Metab Disord. 2024 Jun;25(3):555-573. doi: 10.1007/s11154-023-09868-4. Epub 2023 Dec 19. Rev Endocr Metab Disord. 2024. PMID: 38112850 Review.

5

An in vivo functional assay to characterize human STAT5B genetic variants during zebrafish development.

Landi E, Karabatas L, Rodríguez Gomez T, Salatino L, Scaglia P, Ramírez L, Keselman A, Braslavsky D, Sanguineti N, Pennisi P, Rey RA, Bergadá I, Jasper HG, Domené HM, Plazas PV, Domené S. Landi E, et al. Among authors: keselman a. Hum Mol Genet. 2023 Jul 20;32(15):2473-2484. doi: 10.1093/hmg/ddad078. Hum Mol Genet. 2023. PMID: 37162340

6

Growth follow-up in 100 children with congenital hypothyroidism before and during treatment.

Chiesa A, Gruñeiro de Papendieck L, Keselman A, Heinrich JJ, Bergada C. Chiesa A, et al. Among authors: keselman a. J Pediatr Endocrinol. 1994 Jul-Sep;7(3):211-7. doi: 10.1515/jpem.1994.7.3.211. J Pediatr Endocrinol. 1994. PMID: 7820215 Clinical Trial.

7

Growth of Argentinian girls with Turner syndrome.

Garcia Rudaz C, Martínez AS, Heinrich JJ, Lejarraga H, Keselman A, Laspiur M, Bergadá C. Garcia Rudaz C, et al. Among authors: keselman a. Ann Hum Biol. 1995 Nov-Dec;22(6):533-44. doi: 10.1080/03014469500004192. Ann Hum Biol. 1995. PMID: 8815780 Free article.

8

Final height in long-term primary hypothyroid children.

Chiesa A, Gruñeiro de Papendieck L, Keselman A, Heinrich JJ, Bergadá C. Chiesa A, et al. Among authors: keselman a. J Pediatr Endocrinol Metab. 1998 Jan-Feb;11(1):51-8. doi: 10.1515/jpem.1998.11.1.51. J Pediatr Endocrinol Metab. 1998. PMID: 9642629

9

Psychosocial outcome in growth hormone deficient patients diagnosed during childhood.

Keselman A, Martínez A, Pantano L, Bergadá C, Heinrich JJ. Keselman A, et al. J Pediatr Endocrinol Metab. 2000 Apr;13(4):409-16. doi: 10.1515/jpem.2000.13.4.409. J Pediatr Endocrinol Metab. 2000. PMID: 10776995

10

Height velocity in Argentinean girls with Turner's syndrome.

Lejarraga H, Martínez A, García Rudaz C, Hauspie R, Tibaldi F, Keselman A, Heinrich J. Lejarraga H, et al. Among authors: keselman a. J Pediatr Endocrinol Metab. 2001 Jul-Aug;14(7):883-91. doi: 10.1515/jpem.2001.14.7.883. J Pediatr Endocrinol Metab. 2001. PMID: 11515729

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