Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jaime Sánchez del Pozo"'
Publikováno v:
Anales de Pediatría, Vol 91, Iss 3, Pp 207-208 (2019)
Externí odkaz:
https://doaj.org/article/c3c8cf3d73764d83b2c0485d9369d29d
Autor:
Alba Rubio-San-Simón, Nelly Román Mendoza, Cristina Nova Lozano, Jaime Sánchez del Pozo, Pilar Guerra García
Publikováno v:
Anales de Pediatría, Vol 91, Iss 1, Pp 64-65 (2019)
Externí odkaz:
https://doaj.org/article/0e9dbfa9550c4f15ab059b79aab5006c
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 34:531-534
We present an unusual case of SHOX deficiency associated with Léri-Weill dyschondrosteosis (LWD), Hashimoto’s thyroiditis and pseudohypoparathyroidism 1B in a young woman. To our knowledge, this is the first ever report of these disorders coexisti
Panel Discussion: Some Aspects of the Management of Patients with X-Linked Hypophosphataemic Rickets
Autor:
Jaime Sánchez del Pozo, Jose-Vicente Torregrosa, Manuel Muñoz Torres, María Isabel Luiz Yanes
Publikováno v:
Advances in Therapy. 37:121-126
X-linked hypophosphataemia (XLH) rickets is a rare disease frequently misdiagnosed and mismanaged. Despite having clinical guidelines that offers some therapeutic recommendations based on the clinical experience of experts, physicians still have ques
Publikováno v:
Anales de Pediatría, Vol 91, Iss 3, Pp 207-208 (2019)
Autor:
María Isabel Luiz Yanes, Manuel Muñoz Torres, Jose-Vicente Torregrosa, Jaime Sánchez del Pozo
Publikováno v:
Advances in Therapy. 37:3432-3432
In the original article, third author name has been published incorrectly.
Autor:
Alba, Rubio-San-Simón, Nelly, Román Mendoza, Cristina, Nova Lozano, Jaime, Sánchez Del Pozo, Pilar, Guerra García
Publikováno v:
Anales de pediatria. 91(1)
Publikováno v:
Anales de pediatria. 91(3)
Autor:
Nelly Marlene Román Mendoza, Alba Rubio-San-Simón, Cristina Nova Lozano, Pilar Guerra García, Jaime Sánchez Del Pozo
Publikováno v:
Anales de Pediatría, Vol 91, Iss 1, Pp 64-65 (2019)
Autor:
Jaime Sánchez del Pozo, Alessia David, Andrew Dauber, Philippe Backeljauw, Martin O. Savage, Merve Emecen Sanli, Lina Merjaneh, Louise A. Metherell, Kanimozhi Vairamani, Ron G. Rosenfeld, Paula Casano-Sancho, Vivian Hwa, Javier Aisenberg
Publikováno v:
Journal of the Endocrine Society
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Context: Autosomal-recessive mutations in the growth hormone receptor (GHR) are the most common causes for primary growth hormone insensitivity (GHI) syndrome with classical GHI phenotypically characterized by severe short stature and marked insulin-