Chiesa A - Search Results

1

17alpha-hydroxyprogesterone and cortisol serum levels in neonates and young children: influence of age, gestational age, gender and methodological procedures.

Ballerini MG, Chiesa A, Scaglia P, Gruñeiro-Papendieck L, Heinrich JJ, Ropelato MG. Ballerini MG, et al. Among authors: chiesa a. J Pediatr Endocrinol Metab. 2010 Jan-Feb;23(1-2):121-32. doi: 10.1515/jpem.2010.23.1-2.121. J Pediatr Endocrinol Metab. 2010. PMID: 20432815

2

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. 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.

3

Final height in long-term primary hypothyroid children.

Chiesa A, Gruñeiro de Papendieck L, Keselman A, Heinrich JJ, Bergadá C. Chiesa A, et al. 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

4

Nocturnal TSH surge and TRH test response in the evaluation of thyroid axis in hypothalamic pituitary disorders in childhood.

Gruñeiro-Papendieck L, Chiesa A, Martínez A, Heinrich JJ, Bergadá C. Gruñeiro-Papendieck L, et al. Among authors: chiesa a. Horm Res. 1998;50(5):252-7. doi: 10.1159/000023286. Horm Res. 1998. PMID: 9873192 Clinical Trial.

5

Usefulness of thyroxine and free thyroxine filter paper measurements in neonatal screening for congenital hypothyroidism of preterm babies.

Gruñeiro-Papendieck L, Prieto L, Chiesa A, Bengolea S, Bossi G, Bergadá C. Gruñeiro-Papendieck L, et al. Among authors: chiesa a. J Med Screen. 2000;7(2):78-81. doi: 10.1136/jms.7.2.78. J Med Screen. 2000. PMID: 11002447

6

Neonatal screening program for congenital adrenal hyperplasia: adjustments to the recall protocol.

Gruñeiro-Papendieck L, Prieto L, Chiesa A, Bengolea S, Bossi G, Bergadá C. Gruñeiro-Papendieck L, et al. Among authors: chiesa a. Horm Res. 2001;55(6):271-7. doi: 10.1159/000050012. Horm Res. 2001. PMID: 11805430

7

Thyroid dysfunction and high thyroid stimulating hormone levels in children with Down's syndrome.

Gruñeiro de Papendieck L, Chiesa A, Bastida MG, Alonso G, Finkielstain G, Heinrich JJ. Gruñeiro de Papendieck L, et al. Among authors: chiesa a. J Pediatr Endocrinol Metab. 2002 Nov-Dec;15(9):1543-8. doi: 10.1515/jpem.2002.15.9.1543. J Pediatr Endocrinol Metab. 2002. PMID: 12503863

8

Congenital secondary hypothyroidism due to a mutation C105Vfs114X thyrotropin-beta mutation: genetic study of five unrelated families from Switzerland and Argentina.

Deladoëy J, Vuissoz JM, Domené HM, Malik N, Gruneiro-Papendieck L, Chiesa A, Heinrich JJ, Mullis PE. Deladoëy J, et al. Among authors: chiesa a. Thyroid. 2003 Jun;13(6):553-9. doi: 10.1089/105072503322238818. Thyroid. 2003. PMID: 12930599

9

Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect.

Rivolta CM, Esperante SA, Gruñeiro-Papendieck L, Chiesa A, Moya CM, Domené S, Varela V, Targovnik HM. Rivolta CM, et al. Among authors: chiesa a. Hum Mutat. 2003 Sep;22(3):259. doi: 10.1002/humu.9175. Hum Mutat. 2003. PMID: 12938097

10

The C105fs114X is the prevalent thyrotropin beta-subunit gene mutation in Argentinean patients with congenital central hypothyroidism.

Domené HM, Gruñeiro-Papendieck L, Chiesa A, Iorcansky S, Herzovich VC, Papazian R, Forclaz V, Prieto L, Sansó G, Scaglia P, Bre M, Chamoux A, Heinrich JJ. Domené HM, et al. Among authors: chiesa a. Horm Res. 2004;61(1):41-6. doi: 10.1159/000075196. Epub 2003 Nov 27. Horm Res. 2004. PMID: 14646401

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