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1. Hypomorphic variants of SEL1L-HRD1 ER-associated degradation are associated with neurodevelopmental disorders

2. SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability

5. Hypomorphic variants of SEL1L-HRD1 ER-associated degradation are associated with neurodevelopmental disorders

6. PRPS1 loss-of-function variants, from isolated hearing loss to severe congenital encephalopathy: New cases and literature review

9. IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

10. Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder

12. Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

15. Biallelic IARS2 mutations presenting as sideroblastic anemia

17. Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease

18. Mutations in BOREALIN cause thyroid dysgenesis

19. Mutations inHID1Cause Syndromic Infantile Encephalopathy and Hypopituitarism

20. Mutations in HID1 Cause Syndromic Infantile Encephalopathy and Hypopituitarism

21. Mutations in the tricarboxylic acid cycle enzyme, aconitase 2, cause either isolated or syndromic optic neuropathy with encephalopathy and cerebellar atrophy

22. Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?

23. Biallelic IARS2 mutations presenting as sideroblastic anemia

24. Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?

25. YIF1B mutations cause a post-natal neurodevelopmental syndrome associated with Golgi and primary cilium alterations

26. Developmental and epilepsy spectrum of KCNB1 encephalopathy with long‐term outcome

28. Evidence of diaphragmatic dysfunction with severe alveolar hypoventilation syndrome in mitochondrial respiratory chain deficiency

30. Vingt ans de consultations de génétique clinique sur site dans les hôpitaux de jour pour les personnes atteintes de troubles du spectre autistique de la région parisienne

32. Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injection

36. Novel GABRA2 variants in epileptic encephalopathy and intellectual disability with seizures

37. TUBB 1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology

38. Evaluation of methods for amplification of picogram amounts of total RNA for whole genome expression profiling

39. A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations

40. De novo SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizures.

42. High predictive value of brain MRI imaging in primary mitochondrial respiratory chain deficiency

43. A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations

46. Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies

47. Mutations in BOREALIN cause thyroid dysgenesis

48. Mosaicism in ATP1A3-related disorders: not just a theoretical risk

49. De novoSCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizures

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