Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Ectopic neurohypophysis"'
Autor:
Dulika Sumathipala, Petter Strømme, Christian Gilissen, Ingunn Holm Einarsen, Hilde J. Bjørndalen, Andrés Server, Jordi Corominas, Bjørnar Hassel, Madeleine Fannemel, Doriana Misceo, Eirik Frengen
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Joubert syndrome (JBTS) is a genetically heterogeneous group of neurodevelopmental syndromes caused by primary cilia dysfunction. Usually the neurological presentation starts with abnormal neonatal breathing followed by muscular h
Externí odkaz:
https://doaj.org/article/f92a324c5fd24435bbc9013132144230
Autor:
Deep Dutta, Ajitesh Roy, Sujoy Ghosh, Pradip Mukhopadhyay, Ranen Dasgupta, Satinath Mukhopadhyay, Subhankar Chowdhury
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 8, Pp 288-290 (2012)
Ectopic neurohypophysis (EN) is found in nearly half of children with growth hormone deficiency (GHD). Rathke′s cyst (RC) is uncommon in children and when present, hypopituitarism is found in nearly half of them. We present a fourteen and half-year
Externí odkaz:
https://doaj.org/article/bf88f139f9534483ab6f42fd58c56d52
Publikováno v:
The Turkish Journal of Endocrinology and Metabolism. 23:77-84
Objective: Ectopic posterior pituitary (EPP) can occur because of a migration defect or neurodegeneration of the hypothalamic nuclei. EPP is typically rarely diagnosed. Therefore, we aimed to report our patients with EPP. Material and Methods: This i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0382cf407ca563fe424d7595cf4ecd13
https://hdl.handle.net/11454/69605
https://hdl.handle.net/11454/69605
Autor:
Gail Louise Nunlee-Bland, Wolali Akua-Sabia Odonkor, Vijaya A Ganta, Anteneh Woldetensay Zenebe, Nada Osman, MaKenzie Hodge, kehinde Matilda folawewo
Publikováno v:
Journal of the Endocrine Society
Pituitary stalk interruption syndrome (PSIS) is a congenital disorder of the pituitary gland. Symptoms at presentation may vary widely as this disease presents along a spectrum which includes; ectopic posterior pituitary, interrupted pituitary stalk
Autor:
Madeleine Fannemel, Dulika S. Sumathipala, Andres Server, Bjørnar Hassel, Christian Gilissen, Ingunn Holm Einarsen, Hilde Johanne Bjørndalen, Eirik Frengen, Doriana Misceo, Petter Strømme, Jordi Corominas
Publikováno v:
BMC Medical Genetics, 21
BMC Medical Genetics, 21, 1
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
BMC Medical Genetics
BMC Medical Genetics, 21, 1
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
BMC Medical Genetics
Background Joubert syndrome (JBTS) is a genetically heterogeneous group of neurodevelopmental syndromes caused by primary cilia dysfunction. Usually the neurological presentation starts with abnormal neonatal breathing followed by muscular hypotonia,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::639132d8097416bb953c43081a412b7a
http://hdl.handle.net/2066/220478
http://hdl.handle.net/2066/220478
Autor:
Vatan Barisik, Hüseyin Anıl Korkmaz, Utku Karaarslan, Dinçer Atila, Filiz Hazan, C Eraslan, Behzat Özkan, Melek Yildiz, Ozdal Etlik, E S Ata
Publikováno v:
ResearcherID
WOS: 000451246700003
PubMed ID: 31149275
Objective. Ectopic posterior pituitary gland (EPP) is usually characterized by an abnormal pituitary stalk and hypoplasia of the anterior hypophysis. The genetic mechanisms involved in the developmen
PubMed ID: 31149275
Objective. Ectopic posterior pituitary gland (EPP) is usually characterized by an abnormal pituitary stalk and hypoplasia of the anterior hypophysis. The genetic mechanisms involved in the developmen
Publikováno v:
Endocrine Abstracts.
Objective: To evaluate the importance of magnetic resonance imaging in the treatment and follow-up of patients with pituitary stalk interruption syndrome. Material and Methods: The study included patients who were admitted to the Endocrinology and Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4778::62e06a6c32c19eca4b19d20d29a2c4b2
https://hdl.handle.net/20.500.12483/3022
https://hdl.handle.net/20.500.12483/3022
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