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Diagnosis and approach of pseudohypoparathyroidism type 1A and related disorders during long term follow-up: a case report.
J Pediatr Endocrinol Metab. 2024 Feb 5;37(3):289-295. doi: 10.1515/jpem-2023-0454. Print 2024 Mar 25.
J Pediatr Endocrinol Metab. 2024.
PMID: 38353264
TSH elevation in neonatal screening as the first manifestation of other associated diseases.
Rodríguez Del Rosario S, Gutiérrez Zamorano M, Pérez de Nanclares Leal G, Rellán Rodríguez S, Bahíllo-Curieses MP.
Rodríguez Del Rosario S, et al. Among authors: perez de nanclares leal g.
Endocrinol Diabetes Nutr (Engl Ed). 2023 Apr;70(4):297-299. doi: 10.1016/j.endien.2023.03.017. Epub 2023 Apr 4.
Endocrinol Diabetes Nutr (Engl Ed). 2023.
PMID: 37024330
No abstract available.
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[Familial hypocalciuric hypercalcemia: a new mutation].
Ubetagoyena Arrieta M, Castaño González L, Pérez de Nanclares Leal G, Arruebarrena Lizarraga D, Imaz Murguiondo M, Areses Trapote R.
Ubetagoyena Arrieta M, et al. Among authors: perez de nanclares leal g.
An Pediatr (Barc). 2011 Jan;74(1):47-50. doi: 10.1016/j.anpedi.2010.10.001. Epub 2010 Dec 24.
An Pediatr (Barc). 2011.
PMID: 21185797
Free article.
Spanish.
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A new dominant branchiogenic-deafness syndrome with internal auditory canal hypoplasia and abnormal extremities.
Mégarbané A, Rassi S, Chouery E, Delague V, Perez de Nanclares Leal G, Tabet M, Castaño L, Loiselet J.
Mégarbané A, et al. Among authors: perez de nanclares leal g.
Am J Med Genet A. 2003 Jul 15;120A(2):276-82. doi: 10.1002/ajmg.a.20077.
Am J Med Genet A. 2003.
PMID: 12833414
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