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HLA Region Gene Involvement in Congenital Hypothyroidism
Thyroid Autoimmunity
◽
10.1007/978-1-4613-0945-1_84
◽
1987
◽
pp. 477-479
Author(s):
Mariangela Cisternino
◽
Miryam Martinetti
◽
Renata Lorini
◽
Angelo Gruppioni
◽
Daniela Larizza
◽
...
Keyword(s):
Congenital Hypothyroidism
◽
Region Gene
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INCIDENCE OF CONGENITAL HYPOTHYROIDISM. A RETROSPECTIVE STUDY COMPARING NEONATAL SCREENING AND CLINICAL DIAGNOSIS.
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10.1530/acta.0.103s058
◽
1983
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pp. S58-S61
Author(s):
A Larsson
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L Haganfeldt
◽
J Aim
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K Lundberg
Keyword(s):
Retrospective Study
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Congenital Hypothyroidism
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Neonatal Screening
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An audit to assess the impact of increasing the borderline blood spot TSH cut-off on the detection of cases of congenital hypothyroidism (CHT) identified via newborn screening
Endocrine Abstracts
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10.1530/endoabs.36.p82
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2014
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Newborn Screening
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Congenital Hypothyroidism
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The Impact
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Blood Spot
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The impact of receiving a diagnosis of congenital hypothyroidism on families
Endocrine Abstracts
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10.1530/endoabs.36.oc5.2
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2014
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Author(s):
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Julia Priestley
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Jenny Walker
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Keyword(s):
Congenital Hypothyroidism
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The Impact
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Treatment of congenital hypothyroidism
Endocrine Abstracts
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10.1530/endoabs.49.mte4
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2017
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Author(s):
Heiko Krude
Keyword(s):
Congenital Hypothyroidism
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Is there a place for Thyroid Scintigraphy with Technetium 99 m in the exploration of congenital hypothyroidism in the absence of Iode 123
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10.1530/endoabs.70.aep987
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Newborn screening in Nigeria: Will incorporating congenital hypothyroidism with sickle cell disease improve neonatal screening programme?
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Newborn Screening
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Congenital Hypothyroidism
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Neonatal Screening
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Screening Programme
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Incidence of congenital hypothyroidism over 37 Years in Ireland
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10.1530/ey.16.3.7
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2019
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Author(s):
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◽
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Faculty Opinions recommendation of Update of newborn screening and therapy for congenital hypothyroidism.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.1040032.488940
◽
2006
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Author(s):
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Newborn Screening
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Faculty Opinions recommendation of Nineteen years of national screening for congenital hypothyroidism: familial cases with thyroid dysgenesis suggest the involvement of genetic factors.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.724098926.793503202
◽
2015
◽
Author(s):
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◽
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Familial Cases
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