Martul P - Search Results

1

Molecular analysis of hereditary hyperferritinemia-cataract syndrome in a large Basque family.

Pérez de Nanclares G, Castaño L, Martul P, Rica I, Vela A, Sanjurjo P, Aldamiz-Echevarría K, Martínez R, Sarrionandia MJ. Pérez de Nanclares G, et al. Among authors: martul p. J Pediatr Endocrinol Metab. 2001 Mar;14(3):295-300. doi: 10.1515/jpem.2001.14.3.295. J Pediatr Endocrinol Metab. 2001. PMID: 11308047

2

Molecular analysis of Frasier syndrome: mutation in the WT1 gene in a girl with gonadal dysgenesis and nephronophthisis.

Pérez de Nanclares G, Castaño L, Bilbao JR, Vallo A, Rica I, Vela A, Martul P. Pérez de Nanclares G, et al. Among authors: martul p. J Pediatr Endocrinol Metab. 2002 Jul-Aug;15(7):1047-50. doi: 10.1515/jpem.2002.15.7.1047. J Pediatr Endocrinol Metab. 2002. PMID: 12199335

3

Panhypopituitarism: genetic versus acquired etiological factors.

Coya R, Vela A, Pérez de Nanclares G, Rica I, Castaño L, Busturia MA, Martul P; GEDPIT group. Coya R, et al. Among authors: martul p. J Pediatr Endocrinol Metab. 2007 Jan;20(1):27-36. doi: 10.1515/jpem.2007.20.1.27. J Pediatr Endocrinol Metab. 2007. PMID: 17315526

4

Absence of diabetes mellitus type 2 in obese children and adolescents in the north of Spain.

Aguayo A, Vela A, Aniel-Quiroga A, Blarduni E, Fernández C, Grau G, Núñez J, Martul P, Castaño L, Rica I. Aguayo A, et al. Among authors: martul p. J Pediatr Endocrinol Metab. 2013;26(1-2):25-9. doi: 10.1515/jpem-2012-0200. J Pediatr Endocrinol Metab. 2013. PMID: 23329743

5

Dual growth hormone (GH) response to repeated GH releasing hormone stimulus in children and adults.

Vela A, Algorta J, Martul P, Coya R, Rica I, Aniel-Quiroga MA, Busturia MA. Vela A, et al. Among authors: martul p. J Pediatr Endocrinol Metab. 2004 May;17(5):743-8. doi: 10.1515/jpem.2004.17.5.743. J Pediatr Endocrinol Metab. 2004. PMID: 15237709 Clinical Trial.

6

Clinical evaluation and health care in childhood and adolescent obesity.

Martul P, Rica I, Vela A, Aguayo A. Martul P, et al. J Pediatr Endocrinol Metab. 2005 Dec;18 Suppl 1:1207-13. doi: 10.1515/JPEM.2005.18.s1.1207. J Pediatr Endocrinol Metab. 2005. PMID: 16398451 Review. No abstract available.

7

Heterogeneity of vitamin D receptor gene association with celiac disease and type 1 diabetes mellitus.

San-Pedro JI, Bilbao JR, Perez de Nanclares G, Vitoria JC, Martul P, Castaño L. San-Pedro JI, et al. Among authors: martul p. Autoimmunity. 2005 Sep;38(6):439-44. doi: 10.1080/08916930500288455. Autoimmunity. 2005. PMID: 16278149 Free article.

8

Urinary iodine and thyroid function in a population of healthy pregnant women in the North of Spain.

Aguayo A, Grau G, Vela A, Aniel-Quiroga A, Espada M, Martul P, Castaño L, Rica I. Aguayo A, et al. Among authors: martul p. J Trace Elem Med Biol. 2013 Oct;27(4):302-6. doi: 10.1016/j.jtemb.2013.07.002. Epub 2013 Jul 16. J Trace Elem Med Biol. 2013. PMID: 23992867

9

Functional study of a novel single deletion in the TITF1/NKX2.1 homeobox gene that produces congenital hypothyroidism and benign chorea but not pulmonary distress.

Moya CM, Perez de Nanclares G, Castaño L, Potau N, Bilbao JR, Carrascosa A, Bargadá M, Coya R, Martul P, Vicens-Calvet E, Santisteban P. Moya CM, et al. Among authors: martul p. J Clin Endocrinol Metab. 2006 May;91(5):1832-41. doi: 10.1210/jc.2005-1497. Epub 2006 Feb 28. J Clin Endocrinol Metab. 2006. PMID: 16507635 Free article.

10

Oral dexamethasone administration: new pharmacological test for the assessment of growth hormone secretion.

Pineda J, Martul P, Casanueva FF, Dieguez C, Rica I, Loridan L. Pineda J, et al. Among authors: martul p. Eur J Endocrinol. 1994 Dec;131(6):598-601. doi: 10.1530/eje.0.1310598. Eur J Endocrinol. 1994. PMID: 7804442 Clinical Trial.

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