(Q47341299)

14 January 2018

title

Untreated hypopituitarism due to absence of the pituitary stalk with normal adult height: report of two cases (English)

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14 January 2018

author name string

Leda Papastathopoulou

1

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14 January 2018

Marinella Tzanela

2

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14 January 2018

Vania Vlassopoulou

3

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14 January 2018

Dimitra Vassiliadi

4

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14 January 2018

Nikolaos Thalassinos

5

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14 January 2018

publication date

1 February 2006

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14 January 2018

published in

Endocrine

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14 January 2018

volume

29

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14 January 2018

issue

1

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14 January 2018

page(s)

175-179

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14 January 2018

https://scigraph.springernature.com/pub.10.1385/endo:29:1:175

exact match

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cites work

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Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: summary statement of the GH Research Society. GH Research Society

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Normal growth in a patient with septo-optic dysplasia despite both growth hormone and IGF-I deficiency

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Dynamic MRI in the congenital agenesis of the neural pituitary stalk syndrome: the role of the vascular pituitary stalk in predicting residual anterior pituitary function.

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Near-normal linear growth in the setting of markedly reduced growth hormone and IGF-1. A case report

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Molecular analysis of LHX3 and PROP-1 in pituitary hormone deficiency patients with posterior pituitary ectopia

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Insulin as a growth factor

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A 43-year-old male with untreated panhypopituitarism due to absence of the pituitary stalk: from dwarf to giant

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Leptin acts as a growth factor on the chondrocytes of skeletal growth centers

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A unique growth factor in patients with acromegaloidism

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Normal growth despite GH, IGF-I and IGF-II deficiency

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Growth without growth hormone (GH): a case report

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Gene symbol: TSH B. Disease: congenital hypothyroidism

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Congenital hypopituitarism in a 48-year old adult. Natural course, hormonal study and MRI evidence

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Pituitary magnetic resonance imaging in 15 patients with Prop1 gene mutations: pituitary enlargement may originate from the intermediate lobe

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Panhypopituitarism associated with severe retroperitoneal fibrosis

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Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene

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A hypopituitary patient who attained tall stature without growth hormone

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Do all patients with childhood-onset growth hormone deficiency (GHD) and ectopic neurohypophysis have persistent GHD in adulthood?

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A patient of hypogonadotropic hypogonadism accompanied by growth hormone deficiency and decreased bone mineral density who attained normal growth

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Adult height in growth hormone (GH)-deficient children treated with biosynthetic GH. The Genentech Growth Study Group

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Growth without growth hormone: the "invisible" GH syndrome

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Estrogenic antagonism of metabolic effects of administered growth hormone

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Identifiers

DOI

10.1385/ENDO:29:1:175

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14 January 2018

Dimensions Publication ID

1004884262

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14 January 2018