rdf:type |
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lifeskim:mentions |
|
pubmed:issue |
6
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pubmed:dateCreated |
2007-6-7
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pubmed:databankReference |
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pubmed:abstractText |
Several endocrine disorders that share resistance to PTH are grouped under the term pseudohypoparathyroidism (PHP). PHP type I, associated with blunted PTH-induced nephrogenous cAMP formation and phosphate excretion, is subdivided according to the presence or absence of additional endocrine abnormalities, Albright's hereditary osteodystrophy (AHO), and reduced Gsalpha activity caused by GNAS mutations.
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pubmed:grant |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
AIM
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pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0021-972X
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pubmed:author |
pubmed-author:AhrensWiebkeW,
pubmed-author:BarrosFranciscoF,
pubmed-author:BastepeMuratM,
pubmed-author:BilbaoJosé RamónJR,
pubmed-author:CastañoLuisL,
pubmed-author:Fernández-RebolloEduardoE,
pubmed-author:García-CuarteroBeatrizB,
pubmed-author:GaztambideSoniaS,
pubmed-author:HiortOlafO,
pubmed-author:JüppnerHaraldH,
pubmed-author:MenéndezEdelmiroE,
pubmed-author:MoralesMaria JoseMJ,
pubmed-author:PomboManuelM,
pubmed-author:SantinIzortzeI,
pubmed-author:ZazoNuriaN,
pubmed-author:de NanclaresGuiomar PérezGP
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pubmed:issnType |
Print
|
pubmed:volume |
92
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
2370-3
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17405843-Adult,
pubmed-meshheading:17405843-Epigenesis, Genetic,
pubmed-meshheading:17405843-Female,
pubmed-meshheading:17405843-Fibrous Dysplasia, Polyostotic,
pubmed-meshheading:17405843-GTP-Binding Protein alpha Subunits, Gs,
pubmed-meshheading:17405843-Humans,
pubmed-meshheading:17405843-Infant,
pubmed-meshheading:17405843-Metacarpal Bones,
pubmed-meshheading:17405843-Phenotype,
pubmed-meshheading:17405843-Pseudohypoparathyroidism,
pubmed-meshheading:17405843-Severity of Illness Index
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pubmed:year |
2007
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pubmed:articleTitle |
Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright's hereditary osteodystrophy.
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pubmed:affiliation |
Endocrinology and Diabetes Research Group, Hospital de Cruces, Cruces-Barakaldo E48903 Bizkaia, Basque Country, Spain.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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