scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1365-2265.2006.02692.X |
P698 | PubMed publication ID | 17201807 |
P50 | author | Berenice Bilharinho Mendonça | Q42957618 |
Luciani Renata Carvalho | Q45750114 | ||
P2093 | author name string | Claudia Costa Leite | |
Mirta Knoepfelmacher | |||
Suemi Marui | |||
Ivo Jorge Prado Arnhold | |||
Maria Edna Melo | |||
P2860 | cites work | Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Q24323305 |
Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism | Q24531513 | ||
Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4. | Q24536132 | ||
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency | Q28145571 | ||
Evaluation of adrenal function in patients with growth hormone deficiency and hypothalamic-pituitary disorders: comparison between insulin-induced hypoglycemia, low-dose ACTH, standard ACTH and CRH stimulation tests | Q28249181 | ||
LIM homeodomain factors Lhx3 and Lhx4 assign subtype identities for motor neurons | Q28591209 | ||
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GH values after clonidine stimulation measured by immunofluorometric assay in normal prepubertal children and GH-deficient patients | Q44417408 | ||
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Prevalence of adrenocorticotropin deficiency in children with idiopathic growth hormone deficiency | Q45241654 | ||
Height of normal pituitary gland as a function of age evaluated by magnetic resonance imaging in children | Q47436393 | ||
Growth hormone deficiency with ectopic neurohypophysis: anatomical variations and relationship between the visibility of the pituitary stalk asserted by magnetic resonance imaging and anterior pituitary function | Q48164255 | ||
Transection of the pituitary stalk: development of an ectopic posterior lobe assessed with MR imaging | Q48186960 | ||
Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes | Q48454502 | ||
The association of hypopituitarism with small pituitary, invisible pituitary stalk, type 1 Arnold-Chiari malformation, and syringomyelia in seven patients born in breech position: a further proof of birth injury theory on the pathogenesis of "idiopa | Q48499854 | ||
Multistep control of pituitary organogenesis | Q48577432 | ||
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 | Q48923277 | ||
Diagnostic Value of Fluorometric Assays in the Evaluation of Precocious Puberty | Q57632825 | ||
P433 | issue | 1 | |
P304 | page(s) | 95-102 | |
P577 | publication date | 2007-01-01 | |
P1433 | published in | Clinical Endocrinology | Q15762781 |
P1476 | title | Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe | |
P478 | volume | 66 |
Q35553223 | Candidate genes for panhypopituitarism identified by gene expression profiling |
Q51627755 | Detection of genetic hypopituitarism in an adult population of idiopathic pituitary insufficiency patients with growth hormone deficiency. |
Q45921010 | Effects of genetic variability of the caprine homeobox transcription factor HESX1 gene on performance traits. |
Q38797075 | Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era. |
Q36840767 | Growth Hormone Therapy Benefits Pituitary Stalk Interruption Syndrome Patients with Short Stature: A Retrospective Study of 75 Han Chinese |
Q53447605 | Heterozygous mutation of HESX1 causing hypopituitarism and multiple anatomical malformations without features of septo-optic dysplasia. |
Q47114568 | Multi-genic pattern found in rare type of hypopituitarism: a whole-exome sequencing study of Han Chinese with pituitary stalk interruption syndrome |
Q98177844 | NBPF9 Gene May Be Involved in Congenital Hypopituitarism: A Whole-Genome Study of a Boy with Pituitary Stalk Interruption Syndrome and His Family |
Q35839986 | Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial Presentation |
Q34544745 | Pituitary stalk interruption syndrome in 53 postpubertal patients: factors influencing the heterogeneity of its presentation |
Q34201507 | Pituitary stalk interruption syndrome: Case report of three cases with review of literature |
Q92432504 | SCREENING OF PROP-1, LHX2 AND POU1F1 MUTATIONS IN PATIENTS WITH ECTOPIC POSTERIOR PITUITARY GLAND |
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