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1. A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction

3. Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations

8. CCDC115-CDG: A new rare and misleading inherited cause of liver disease

9. A National French consensus on gene lists for the diagnosis of myopathies using next-generation sequencing

13. Clinical features and prognostic factors of listeriosis: the MONALISA national prospective cohort study

14. Abnormal Glycosylation Profile and High Alpha-Fetoprotein in a Patient with Twinkle Variants

17. A Cause of Permanent Ketosis: GLUT-1 Deficiency

18. From splitting GLUT1 deficiency syndromes to overlapping phenotypes

19. ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

21. Clinical, laboratory and molecular findings and long-term follow-up data in 96 French patients with PMM2-CDG (phosphomannomutase 2-congenital disorder of glycosylation) and review of the literature

29. Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations.

33. SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects

39. Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies

40. Expanding the phenotype of X‐linked SSR4–CDG: Connective tissue implications

41. Long term outcome of MPI‐CDG patients on D‐mannose therapy

42. Serum bikunin isoforms in congenital disorders of glycosylation and linkeropathies

43. A Genome-Wide CRISPR-Cas9 Screen Identifies the Dolichol-Phosphate Mannose Synthase Complex as a Host Dependency Factor for Dengue Virus Infection

44. Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

49. International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up

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