Results 221 to 230 of about 26,843 (264)

Clinical and genetic basis of congenital gonadotropin deficiency. [PDF]

Hum Reprod Open
Wang Y, Zhai J, Habibi I, Kolesińska Z, de Azevedo Correa F, Zouaghi Y, Ameti A, Boizot A, Perdices-López C, Todisco T, Niederländer NJ, Acierno JS, Messina A, Santoni F, Pitteloud N.   +14 more
europepmc   +1 more source

Improvements in screening test, diagnosis, and outcomes of children with congenital hypothyroidism: lessons learned from 50 years of newborn screening. [PDF]

Endocrine
Salerno M, Vigone MC, Cassio A, Cavarzere P, Cherubini V, Faienza MF, Gastaldi R, Tuli G, Wasniewska M, Olivieri A.   +9 more
europepmc   +1 more source

Decompensated liver cirrhosis as a rare consequence of long-term untreated panhypopituitarism after craniopharyngioma resection: a case report. [PDF]

Front Endocrinol (Lausanne)
Cui M, Yu Z, Du Q, Guo Z, Chen Y, Liu M, Liu P.   +6 more
europepmc   +1 more source

Loss of pituitary hormone function after stereotactic radiosurgery for pituitary adenomas: mechanisms and management. [PDF]

J Neurooncol
Faraj CA, McCutcheon IE.
europepmc   +1 more source

Recognising pituitary and thyroid dysfunction after craniospinal radiotherapy: an underrecognised mixed endocrine toxicity. [PDF]

Endocrinol Diabetes Metab Case Rep
Slabbynck K, Roels S, Erven K, Everaert E, Coremans P.   +4 more
europepmc   +1 more source

Multiple cutaneous hemangiomas in a patient with combined pituitary hormone deficiency

Journal of Pediatric Endocrinology and Metabolism, 2014
Combined pituitary hormone deficiency (CPHD) refers to a rare heterogeneous group of conditions in which there is a deficiency in at least two anterior pituitary hormones. Patients with POU1F1 mutations show a combined pituitary deficiency with low or absent levels of growth hormone, prolactin, and thyroid-stimulating hormone.
Ayça Aykut, Samim Özen, Huseyin Önay   +2 more
exaly   +5 more sources

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Pituitary transcription factors in the aetiology of combined pituitary hormone deficiency

Best Practice and Research in Clinical Endocrinology and Metabolism, 2011
The somatotropic axis is the central postnatal regulator of longitudinal growth. One of its major components--growth hormone--is produced by the anterior lobe of the pituitary, which also expresses and secretes five additional hormones (prolactin, thyroid stimulating hormone, follicle stimulating hormone, luteinizing hormone, adrenocorticotropic ...
R Pfäffle
exaly   +3 more sources

Clinical Characteristics of Children with Combined Pituitary Hormone Deficiency and the Effects of Growth Hormone Treatment

Klinische Pädiatrie, 2023
Abstract Aim We aimed to describe the clinical characteristics of patients with congenital combined pituitary hormone deficiency (CPHD) and evaluate the first-year growth responses of individuals with CPHD and isolated growth hormone deficiency (IGHD) in order to establish the ...
Özge Besci, Reyhan Deveci Sevim, Kübra Yüksek Acinikli, Korcan Demir, Gönül Çatlı, Bayram Özhan, Tolga Ünüvar, Ahmet Anık, Ayhan Abacı, Ayça Altıncık   +9 more
core   +6 more sources

"Hot Spot" in the PROP1 Gene Responsible for Combined Pituitary Hormone Deficiency

Journal of Clinical Endocrinology & Metabolism, 1999
As pituitary function depends on the integrity of the hypothalamic-pituitary axis, any defect in the development and organogenesis of this gland may account for a form of combined pituitary hormone deficiency (CPHD). Although pit-1 was 1 of the first factors identified as a cause of CPHD in mice, many other homeodomain and transcription factors have ...
Deladoëy, Johnny, Flück Pandey, Christa Emma, Büyükgebiz, A., Kuhlmann, B. V., Eblé, Andrée, Hindmarsh, P. C., Wu, W., Mullis, Primus-Eugen   +7 more
openaire   +5 more sources