Pituitary stalk interruption syndrome: diagnostic delay and sensitivity of the auxological criteria of the growth hormone research society. The pituitary stalk transection syndrome: multifaceted presentation in adulthood. Relationships between neuroradiological and clinical features in apparently idiopathic hypopituitarism. Congenital adenohypophysis aplasia: clinical features and analysis of the transcriptional factors for embryonic pituitary development. Transection of the pituitary stalk: development of an ectopic posterior lobe assessed with MR imaging. Anterior and posterior lobes of the pituitary gland: assessment by 1.
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Pituitary stalk interruption syndrome: diagnostic delay and sensitivity of the auxological criteria of the growth hormone research society. The pituitary stalk transection syndrome: multifaceted presentation in adulthood. Relationships between neuroradiological and clinical features in apparently idiopathic hypopituitarism. Congenital adenohypophysis aplasia: clinical features and analysis of the transcriptional factors for embryonic pituitary development.
Transection of the pituitary stalk: development of an ectopic posterior lobe assessed with MR imaging. Anterior and posterior lobes of the pituitary gland: assessment by 1. Pituitary stalk dysgenesis-induced hypopituitarism in adult patients: prevalence, evolution of hormone dysfunction and genetic analysis.
Magnetic resonance imaging in the diagnosis of growth hormone deficiency. Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms. Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe. Whole-exome sequencing identifies homozygous GPR mutation in a family with pituitary stalk interruption syndrome.
Long-term evolution of endocrine disorders and effect of GH therapy in 35 patients with pituitary stalk interruption syndrome. Pituitary stalk interruption syndrome: cause, clinical manifestations, diagnosis, and management. Pituitary stalk interruption syndrome in 59 children: the value of MRI in assessment of pituitary functions.
Pituitary stalk interruption syndrome in Chinese people: clinical characteristic analysis of 55 cases. Pituitary stalk interruption syndrome and isolated pituitary hypoplasia may be caused by mutations in holoprosencephaly-related genes. Pituitary stalk interruption syndrome in 58 Chinese patients: clinical features and genetic analysis. Pituitary stalk transection syndrome: comparison of clinico-radiological features in adults and children with review of literature.
Phenotypic variability in children with growth hormone deficiency associated with posterior pituitary ectopia. Pituitary stalk interruption syndrome. Pituitary stalk interruption syndrome: a clinical-biological-genetic assessment of its pathogenesis.
The pituitary stalk interruption syndrome: endocrine features and benefits of growth hormone therapy. Growth and adult height in GH-treated children with nonacquired GH deficiency and idiopathic short stature: the influence of pituitary magnetic resonance imaging findings. Factors influencing the growth hormone peak and plasma insulin-like growth factor I in young adults with pituitary stalk interruption syndrome.
Relationship between pituitary stalk PS visibility and the severity of hormone deficiencies: PS interruption syndrome revisited. Hypothalamic-pituitary function in growth hormone-deficient patients with pituitary stalk transection.
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. Hypothalamic-pituitary vascularization in pituitary stalk transection syndrome: is the pituitary stalk really transected? Case pituitary stalk transection syndrome with ectopic posterior pituitary gland.
Subhypothalamic high-intensity signals identified by magnetic resonance imaging in children with idiopathic anterior hypopituitarism. Gonadotrophic status in adolescents with pituitary stalk interruption syndrome.
MRI of the hypothalamic-pituitary axis in children. Cruikshank DP. Breech presentation. Hypopituitarism and stalk agenesis: a congenital syndrome worsened by breech delivery?
Clinical analysis of 13 cases with growth hormone deficiency combined with pituitary stalk interruption. Survey studies on pituitary diseases in Japan.
Hypothalamic-pituitary functions in patients with idiopathic pituitary dwarfism. Relationship between cesarean delivery rate and maternal and neonatal mortality. Genetic screening of combined pituitary hormone deficiency: experience in patients. PROKR2 variants in multiple hypopituitarism with pituitary stalk interruption.
A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency. Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort. A nonsense mutation in the hedgehog receptor CDON associated with pituitary stalk interruption syndrome.
Clinical and molecular aspects of congenital isolated hypogonadotropic hypogonadism. New understandings of the genetic basis of isolated idiopathic central hypogonadism. Pituitary gland development and disease: from stem cell to hormone production.
Molecular mechanisms of pituitary organogenesis: in search of novel regulatory genes. Genetic regulation of pituitary gland development in human and mouse. Genetic aspects of hypothalamic and pituitary gland development. WNT signaling affects gene expression in the ventral diencephalon and pituitary gland growth. Notch signaling in postnatal pituitary expansion: proliferation, progenitors, and cell specification. Developmental regulation of Notch signaling genes in the embryonic pituitary: Prop1 deficiency affects Notch2 expression.
Hedgehog signaling is required for pituitary gland development. NKX2 gene expression in neuroectoderm but not in mesendodermally derived structures depends on sonic hedgehog in mouse embryos.
Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
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