Search

Your search keyword '"Yamasaki, Mami"' showing total 280 results

Search Constraints

Start Over You searched for: Author "Yamasaki, Mami" Remove constraint Author: "Yamasaki, Mami"
280 results on '"Yamasaki, Mami"'

Search Results

1. X-Linked Hydrocephalus

4. Significance of molecular classification of ependymomas: C11orf95-RELA fusion-negative supratentorial ependymomas are a heterogeneous group of tumors

8. IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis

20. Phenotypic Spectrum of COL4A1 Mutations: Porencephaly to Schizencephaly

24. Detection of Transient Increase of Cerebral Blood Flow and Reversible Neuronal Dysfunction by Iodine-123-Iomazenil Single Photon Emission Computed Tomography After Cerebral Hyperperfusion Syndrome After Revascularization Surgery for Moyamoya Disease

31. Additional file 12: of Significance of molecular classification of ependymomas: C11orf95-RELA fusion-negative supratentorial ependymomas are a heterogeneous group of tumors

32. A New X-Linked Mental Retardation Syndrome with Diplegia and Delayed Myelination

33. Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis

36. A case of optic-nerve hypoplasia and anterior segment abnormality associated with facial cleft

37. Additional file 10: of In vitro characterization of neurite extension using induced pluripotent stem cells derived from lissencephaly patients with TUBA1A missense mutations

38. Additional file 1: Table S1. of In vitro characterization of neurite extension using induced pluripotent stem cells derived from lissencephaly patients with TUBA1A missense mutations

39. ATIM-22. ADOPTIVE IMMUNOTHERAPY USING LYMPHOKINE-ACTIVATED αβ T-CELLS IMPROVES TEMOZOLOMIDE-INDUCED LYMPHOPENIA IN PATIENTS WITH GLIOMA

41. Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement

42. Novel MCA/ID syndrome with ASH1L mutation

43. A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly

46. A case of optic-nerve hypoplasia and anterior segment abnormality associated with facial cleft

47. Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability

49. Novel compound heterozygous variants in PLK4 identified in a patient with autosomal recessive microcephaly and chorioretinopathy

50. In vitro characterization of neurite extension using induced pluripotent stem cells derived from lissencephaly patients with TUBA1A missense mutations

Catalog

Books, media, physical & digital resources