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884 results on '"Septo-Optic Dysplasia"'

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1. Pituitary deficiencies related to optic nerve hypoplasia and visual acuity.

2. Ectopic Posterior Pituitary and Its Associations with Extrapituitary Intracranial Anomalies.

3. Partial ectopic posterior pituitary: A rare imaging entity with literature review.

4. Central Diabetes Insipidus in Children as a Diagnostic Challenge.

5. Ectopic Posterior Pituitary and Its Associations with Extrapituitary Intracranial Anomalies

6. Septo-optic dysplasia plus syndrome in a 2-year-old child: A case report

8. Displasia septo-óptica plus: reporte de caso para revisar y reconocer esta entidad.

9. Rare encounter: Adult-onset temporal lobe schizencephaly with septo-optic dysplasia - a case report on comprehensive diagnosis and management

10. A Novel De novo Heterozygous Mutation in the SON Gene Associated with Septo-optic Dysplasia: A New Phenotype.

11. Septo-Optic dysplasia

12. Knockout mice with pituitary malformations help identify human cases of hypopituitarism

13. Stress-Induced Oculogyric Crisis in Septo-Optic Dysplasia: Case Report

14. Knockout mice with pituitary malformations help identify human cases of hypopituitarism.

16. Septo-Optic Dysplasia: A Case Series of 33 Patients.

17. Stress-Induced Oculogyric Crisis in Septo-Optic Dysplasia: Case Report.

18. Septo-optic dysplasia associated with chromosome 15q13.3 duplication: a case report

19. Septo-optic dysplasia PLUS syndrome in a 23 years old patient: A case report

20. Adrenal crisis during a trip in a young child with septo-optic dysplasia.

21. Possibilities of the ultrasound method in the diagnosis of pathology of the septal region. Literature review and clinical cases

22. Neurodevelopmental impairments in children with septo-optic dysplasia spectrum conditions: a systematic review

23. Neurodevelopmental impairments in children with septo-optic dysplasia spectrum conditions: a systematic review.

24. Ultrasound assessment of the fetal optic chiasm.

25. Ultrasound assessment of the fetal optic chiasm

26. Congenital Optic Nerve Anomalies

27. Association of prepregnancy body mass index and gestational weight gain on severity of optic nerve hypoplasia.

28. The role of visual evoked potentials in ophthalmological evaluation of a patient with optic nerve hypoplasia in septo-optic dysplasia.

29. Role of Fetal Magnetic Resonance Imaging in Differentiating Isolated Septal Agenesis from Septo-Optic Dysplasia: Case Study and Review.

30. Selected Ophthalmological Features in Children with Septo-Optic Dysplasia and Optic Nerve Hypoplasia.

31. Delineating septo‐optic dysplasia.

32. Isolated Absent Septum Pellucidum: A Retrospective Study of Fetal Diagnosis and Postnatal Outcomes.

33. De Morsier plus syndrome: A rare congenital disorder presenting with adult onset seizure.

34. Hypothesis: By‐products of vascular disruption carried in the CSF affect prenatal brain development.

35. A Novel De novo Heterozygous Mutation in the SON Gene Associated with Septo-optic Dysplasia: A New Phenotype

36. Septo-optic dysplasia plus: A case report for reviewing and recognizing this condition

37. Clinical, laboratory and neuroimaging profile of patient's cohort with septo-optic dysplasia treated at a pediatric university hospital.

39. Septo-optic dysplasia presenting with nystagmus, pseudo-disc edema, and fovea hypoplasia.

40. Novel Genetic Diagnoses in Septo-Optic Dysplasia.

41. Dysplasie septo optique plus: à propos d'un cas.

42. A severe case of Bosch–Boonstra–Schaaf optic atrophy syndrome with a novel description of coloboma and septo‐optic dysplasia, owing to a start codon variant in the NR2F1 gene.

44. Prenatal diagnosis and outcome of fetuses with isolated agenesis of septum pellucidum: cohort study and meta‐analysis.

45. Transient central diabetes insipidus after cranioplasty for craniosynostosis in an infant with septo-optic dysplasia.

46. Antenatal diagnosis of absence of septum pellucidum

47. Direct OPTOS Nerve Size Determination of Prevalent Optic Nerve Hypoplasia in Alaska

48. Septo-optic dysplasia with amniotic band syndrome sequence: a case report

49. [ NFIX gene mutation causes Marshall-Smith syndrome in a pair of identical twins and literature review].

50. Gastroschisis and septo-optic-pituitary dysplasia: Is there an association?

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