Pages that link to "Q49069570"
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The following pages link to Endocrine disorders in septo-optic dysplasia (De Morsier syndrome)--evaluation and follow up of 18 patients (Q49069570):
Displaying 20 items.
- The Optic Nerve Hypoplasia Spectrum: Review of the Literature and Clinical Guidelines (Q30248949) (← links)
- Septo-optic dysplasia/optic nerve hypoplasia: data from the National Cooperative Growth Study (NCGS). (Q30700961) (← links)
- Visually impaired children with posterior ocular malformations: pre- and neonatal data and visual functions (Q30811695) (← links)
- Spectrum of clinical presentations and endocrinological findings of patients with septo-optic dysplasia: a retrospective study (Q30933908) (← links)
- Absence of the septum pellucidum associated with a midline fornical nodule and ventriculomegaly: a report of two cases (Q33879804) (← links)
- HESX1 and Septo-Optic Dysplasia (Q34158374) (← links)
- Neuropathologic research strategies in holoprosencephaly (Q34489252) (← links)
- Genetics of septo-optic dysplasia (Q34640923) (← links)
- Congenital disorders of the optic nerve: excavations and hypoplasia (Q35943994) (← links)
- Growth hormone in the visual system: comparative endocrinology (Q36736527) (← links)
- Prader—Willi syndrome and the hypothalamus (Q41663129) (← links)
- Severe hypernatraemia associated with growth hormone replacement therapy in a patient with septo-optic dysplasia. (Q46349789) (← links)
- Septo-optic dysplasia with congenital hepatic fibrosis (Q48161458) (← links)
- Hypothalamic Peptides in Human Brain Diseases (Q48161714) (← links)
- Optic nerve hypoplasia in cholestatic infants: a multiple case study. (Q48307813) (← links)
- Septo-optic dysplasia and digital anomalies: another observation (Q48512302) (← links)
- Hypopituitarism and neurodevelopmental abnormalities in relation to central nervous system structural defects in children with optic nerve hypoplasia (Q48701755) (← links)
- Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities (Q49653037) (← links)
- Less known aspects of central hypothyroidism: Part 2 - Congenital etiologies (Q57191081) (← links)
- Pediatric outcome of children with the prenatal diagnosis of isolated septal agenesis (Q64042268) (← links)