Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe

scientific article published in January 2007

Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1111/J.1365-2265.2006.02692.X
P698PubMed publication ID17201807

P50authorBerenice Bilharinho MendonçaQ42957618
Luciani Renata CarvalhoQ45750114
P2093author name stringClaudia Costa Leite
Mirta Knoepfelmacher
Suemi Marui
Ivo Jorge Prado Arnhold
Maria Edna Melo
P2860cites workMutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouseQ24323305
Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarismQ24531513
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 deficiencyQ28145571
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 testsQ28249181
LIM homeodomain factors Lhx3 and Lhx4 assign subtype identities for motor neuronsQ28591209
Magnetic resonance imaging of the hypothalamic-neurohypophyseal systemQ30922242
MR imaging of the pituitary stalk: size, shape, and enhancement patternQ31022720
The occurrence of breech presentation in Norway 1967-1994.Q39467769
GH values after clonidine stimulation measured by immunofluorometric assay in normal prepubertal children and GH-deficient patientsQ44417408
Do all patients with childhood-onset growth hormone deficiency (GHD) and ectopic neurohypophysis have persistent GHD in adulthood?Q45152619
Prevalence of adrenocorticotropin deficiency in children with idiopathic growth hormone deficiencyQ45241654
Height of normal pituitary gland as a function of age evaluated by magnetic resonance imaging in childrenQ47436393
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 functionQ48164255
Transection of the pituitary stalk: development of an ectopic posterior lobe assessed with MR imagingQ48186960
Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genesQ48454502
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 "idiopaQ48499854
Multistep control of pituitary organogenesisQ48577432
Dynamic MRI in the congenital agenesis of the neural pituitary stalk syndrome: the role of the vascular pituitary stalk in predicting residual anterior pituitary functionQ48923277
Diagnostic Value of Fluorometric Assays in the Evaluation of Precocious PubertyQ57632825
P433issue1
P304page(s)95-102
P577publication date2007-01-01
P1433published inClinical EndocrinologyQ15762781
P1476titleHormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe
P478volume66

Reverse relations

cites work (P2860)
Q35553223Candidate genes for panhypopituitarism identified by gene expression profiling
Q51627755Detection of genetic hypopituitarism in an adult population of idiopathic pituitary insufficiency patients with growth hormone deficiency.
Q45921010Effects of genetic variability of the caprine homeobox transcription factor HESX1 gene on performance traits.
Q38797075Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.
Q36840767Growth Hormone Therapy Benefits Pituitary Stalk Interruption Syndrome Patients with Short Stature: A Retrospective Study of 75 Han Chinese
Q53447605Heterozygous mutation of HESX1 causing hypopituitarism and multiple anatomical malformations without features of septo-optic dysplasia.
Q47114568Multi-genic pattern found in rare type of hypopituitarism: a whole-exome sequencing study of Han Chinese with pituitary stalk interruption syndrome
Q98177844NBPF9 Gene May Be Involved in Congenital Hypopituitarism: A Whole-Genome Study of a Boy with Pituitary Stalk Interruption Syndrome and His Family
Q35839986Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial Presentation
Q34544745Pituitary stalk interruption syndrome in 53 postpubertal patients: factors influencing the heterogeneity of its presentation
Q34201507Pituitary stalk interruption syndrome: Case report of three cases with review of literature
Q92432504SCREENING OF PROP-1, LHX2 AND POU1F1 MUTATIONS IN PATIENTS WITH ECTOPIC POSTERIOR PITUITARY GLAND

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