About: Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia

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About: Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 1985

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1985 (uk) im Dezember 1985 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 1985 (ast) scientific article published on 01 December 1985 (en)
publication date	wds:Q69973151-B7EE8F52-9BFD-4BCB-BA6D-4C6BB40AE3A5
publication date	1985-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q69973151-AFFE138A-EF51-4E54-8D22-FA2D5F735815
language of work or name	English
cites work	wds:Q69973151-15A48ED1-9133-42D3-B41A-F27D8533E590 wds:Q69973151-1C6D7183-D8C8-4800-955B-AC8C15E7291F wds:Q69973151-1D2A0635-8788-4FF0-BA7E-16D38BBB339C wds:Q69973151-5B045407-DC8A-42E7-86D9-0F8C57D7F704 wds:Q69973151-5E023901-630E-49F6-99C9-7F796FDF20FF wds:Q69973151-9DCB1641-14CB-4E29-9716-83F7211DC752 wds:Q69973151-B2AA7F87-2F6F-4FF9-85B0-E99BFD8B23D5 wds:Q69973151-C00EAF08-4453-4110-8935-B32F188A5D0B wds:Q69973151-D7339087-1E2F-4050-A0A2-034E5C3BAF0F wds:Q69973151-F7E89C47-4304-465D-8B68-9DA0C3475157 wds:Q69973151-FCB92F5A-0337-41AB-90E2-B9C13BFC29F9
cites work	Congenital Hypothyroidism Associated with Thyrotropin Unresponsiveness and Thyroid Cell Membrane Alterations Defect of Receptor–Cyclase Coupling Protein in Pseudohypoparathyroidism Pseudohypoparathyroidism: defective excretion of 3',5'-AMP in response to parathyroid hormone Pseudohypoparathyroidism type II: a possible defect in the reception of the cyclic AMP signal Pseudohypoparathyroidism type 1a presenting as congenital hypothyroidism Coupling Defect of Thyrotropin Receptor and Adenylate Cyclase in a Pseudohypoparathyroid Patient Congenital hypothyroidism with impaired thyroid response to thyrotropin Characteristics of infantile hypothyroidism discovered on neonatal screening Resistance to multiple hormones in patients with pseudohypoparathyroidism. Association with deficient activity of guanine nucleotide regulatory protein Deficient activity of guanine nucleotide regulatory protein in erythrocytes from patients with pseudohypoparathyroidism Evolution of Skeletal Lesions in Pseudohypoparathyroidism
author name string	wds:Q69973151-2B4E16B5-9E0E-4E7D-9673-BD902A3BA72C wds:Q69973151-BBFFDF10-E6BC-4C6B-BA95-6A0603AC65F6
author name string	W Hung T S Jap
rdfs:label	Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia (en) Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia (nl)
skos:prefLabel	Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia (en) Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia (nl)
name	Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia (en) Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia (nl)
author	wds:Q69973151-A5A90661-CD3D-489D-A121-A2DF3B25CEFC
author	Michael A. Levine
title	wds:Q69973151-83616704-9914-4367-808C-0AA149D04D84
title	Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia (en)
page(s)	wds:Q69973151-9AD26BC1-1A6F-4B3B-827C-D7FE94D3F098
page(s)	919-922
instance of	wds:Q69973151-9D9DC78A-C252-4AFB-AA62-4B9C245655FC
instance of	scholarly article
main subject	wds:Q69973151-6952B55B-94D0-4AEF-8A50-43EB7E168B2E
main subject	Albright's hereditary osteodystrophy
PubMed ID	wds:Q69973151-A169F4E0-E86D-42A9-AF9C-AD6E9B5397C3
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3934357
PubMed ID	3934357
published in	wds:Q69973151-625A6562-F07B-4DDC-8052-2F80D59DA418
published in	The Journal of Pediatrics
issue	wds:Q69973151-47B2801A-146E-4AB8-8986-E786D67C1B45
volume	wds:Q69973151-00942A46-1AB3-4234-AF04-9C251ECA6A0E
issue	6
volume	107
DOI	wds:Q69973151-1420FD9F-6745-407C-8B7A-93FBBE1D4A9B
DOI	http://dx.doi.org/10.1016/S0022-3476(85)80189-X
DOI	10.1016/S0022-3476(85)80189-X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q69973151
is cites work of	Postnatal establishment of allelic Gαs silencing as a plausible explanation for delayed onset of parathyroid hormone resistance owing to heterozygous Gαs disruption Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy. Clinical spectrum and pathogenesis of pseudohypoparathyroidism. Paternal imprinting of Galpha(s) in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a. Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy. Endocrine and molecular biological studies in a German family with Albright hereditary osteodystrophy. Multiple associated endocrine abnormalities in a patient with pseudohypoparathyroidism type 1a Albright's hereditary osteodystrophy Pseudohypoparathyroidism and Gsα-cAMP-linked disorders: current view and open issues. Pseudohypoparathyroidism: one gene, several syndromes Albright's hereditary osteodystrophy Pseudohypoparathyroidism in a mother and son: phenotypic variability and associated disorder Pseudohypoparathyroidism Type 1A-Subclinical Hypothyroidism and Rapid Weight Gain as Early Clinical Signs: A Clinical Review of 10 Cases.
is cites work of	wds:Q38363924-62F0BAB6-0200-4DF2-A3EE-60F5D5BB03DA wds:Q37589286-442BEE33-5F56-41D0-8548-074C5FEAFF08 wds:Q43598330-860194A2-CCFD-4D81-A4AD-CDEEB6C299D9 wds:Q82715980-B76DD44B-C711-4172-A493-7422F3ED3866 wds:Q24517876-27A4F5A4-4EA5-4A4C-AC82-2195D98500C8 wds:Q34437568-F9B8A8F2-E1F2-4E1E-B68C-C977BA484C02 wds:Q48323494-2CC58CD4-0C0F-4D3C-9704-B9C32258F995 wds:Q38816341-9ECFACE2-89CB-4ACA-9605-9735EDBC45D7 wds:Q34547669-248BFC80-3924-435D-9B0C-C717FD798DB2 wds:Q38412094-72183E75-2B65-4646-9BE1-D6E7F8E5A2C6 wds:Q70400506-66E5EAC4-92E1-487D-A96E-F08F53C4BB10 wds:Q33596161-50E84BC0-3E7C-4169-A777-819CAE632364 wds:Q37483952-F1C9F6EB-06F7-463A-8239-048DC5660C8E

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