MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarism.

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Pituitary stalk interruption syndrome in 59 children: the value of MRI in assessment of pituitary functions.Combined pituitary hormone deficiency: current and future status.

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Q30698221-D6013953-E5D1-4229-B805-7BB735D19FFE Q30848681-FD91D421-6DA7-42B4-B4B3-BCC766610DEF

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MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarism.

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2007 nî lūn-bûn

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2007年の論文

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年學術文章

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name

MRI findings and genotype anal ...... h severity of hypopituitarism.

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MRI findings and genotype anal ...... h severity of hypopituitarism.

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MRI findings and genotype anal ...... h severity of hypopituitarism.

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MRI findings and genotype anal ...... h severity of hypopituitarism.

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MRI findings and genotype anal ...... h severity of hypopituitarism.

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MRI findings and genotype anal ...... h severity of hypopituitarism.

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MRI findings and genotype anal ...... h severity of hypopituitarism.

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Anca Zimmermann

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Cecilia Lazea

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Jens-Peter Schenk

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Markus Bettendorf

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Matthias M Weber

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Paula Grigorescu Sido

http://www.w3.org/2001/XMLSchema#string

Roland Pfaffle

http://www.w3.org/2001/XMLSchema#string

Tim Zimmermann

http://www.w3.org/2001/XMLSchema#string

Udo Heinrich

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P2860

Mutations in PROP1 cause familial combined pituitary hormone deficiency

Clinical characteristics and molecular analysis of PIT1, PROP1,LHX3, and HESX1 in combined pituitary hormone deficiency patients with abnormal pituitary MR imaging

PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency

Familial combined pituitary hormone deficiency caused by PROP-1 gene mutation. Growth patterns and MRI studies in untreated subjects

Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency

Use of insulin-like growth factor-binding protein 3 for the evaluation of growth disorders.

Magnetic resonance images of 91 children with different causes of short stature: pituitary size reflects growth hormone secretion.

PROP-1 gene mutation (R120C) causing combined pituitary hormone deficiencies with variable clinical course in eight siblings of one Jewish Moroccan family.

Relationship between the morphological evaluation of the pituitary and the growth hormone (GH) response to GH-releasing hormone Plus arginine in children and adults with congenital hypopituitarism.

Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation.

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587-596

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scholarly article

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10.1515/JPEM.2007.20.5.587

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2007-05-01T00:00:00Z

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17642419

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MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarism.

about

P2860

P2860

MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarism.

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