Genetic forms of hypopituitarism and their manifestation in the neonatal period.
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Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunctionAgenesis of internal carotid artery associated with isolated growth hormone deficiency: a case report and literature reviewRecent advances in central congenital hypothyroidismVisualized gene network reveals the novel target transcripts Sox2 and Pax6 of neuronal development in trans-placental exposure to bisphenol ANestin-Cre mice are affected by hypopituitarism, which is not due to significant activity of the transgene in the pituitary gland.Genetics of isolated growth hormone deficiency.Three Japanese patients with congenital pituitary hormone deficiency and ophthalmological anomalies.Persistent expression of activated notch in the developing hypothalamus affects survival of pituitary progenitors and alters pituitary structure.Variations in PROKR2, but not PROK2, are associated with hypopituitarism and septo-optic dysplasia.All Hormone-Producing Cell Types of the Pituitary Intermediate and Anterior Lobes Derive From Prop1-Expressing Progenitors.Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea.Growth hormone treatment in adults with growth hormone deficiency: the transition.The role of homeodomain transcription factors in heritable pituitary disease.Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.Hospitalisation in Children with Adrenal Insufficiency and Hypopituitarism: Is There a Differential Burden between Boys and Girls and between Age Groups?Case 2: An unusual case of delayed puberty.HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype.Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly.Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency.Central hypothyroidism in adults: better understanding for better care.TRH Action Is Impaired in Pituitaries of Male IGSF1-Deficient Mice.Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects.A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency.NOTCH activity differentially affects alternative cell fate acquisition and maintenance.
P2860
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P2860
Genetic forms of hypopituitarism and their manifestation in the neonatal period.
description
article científic
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article scientifique
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articolo scientifico
@it
artigo científico
@pt
bilimsel makale
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scientific article published on 16 September 2009
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vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Genetic forms of hypopituitarism and their manifestation in the neonatal period.
@en
Genetic forms of hypopituitarism and their manifestation in the neonatal period.
@nl
type
label
Genetic forms of hypopituitarism and their manifestation in the neonatal period.
@en
Genetic forms of hypopituitarism and their manifestation in the neonatal period.
@nl
prefLabel
Genetic forms of hypopituitarism and their manifestation in the neonatal period.
@en
Genetic forms of hypopituitarism and their manifestation in the neonatal period.
@nl
P1476
Genetic forms of hypopituitarism and their manifestation in the neonatal period.
@en
P2093
Kyriaki S Alatzoglou
Mehul T Dattani
P304
P356
10.1016/J.EARLHUMDEV.2009.08.057
P577
2009-09-16T00:00:00Z