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341 results on '"Lumbroso, S."'

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2. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

6. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

16. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

20. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

25. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

26. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

27. CSF-1R mutation is a cause of intracranial cerebral calcifications, cysts, and leukoencephalopathy: mystery case responses

29. Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases

32. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories

33. The IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5a reductase deficiency

34. The IVS1-2A > G mutation in the SRD5A2 gene predominates in Cypriot patients with 5 alpha reductase deficiency

36. Receptors to steroid hormones and aromatase are expressed by cultured motoneurons but not by glial cells from rat embryo spinal cord

42. [Androgen-independent prostate carcinoma and androgen-receptor: recent progress in molecular genetics]

43. Pregnane x Receptor (PXR) expression in colorectal cancer cells restricts irinotecan chemosensitivity through enhanced SN-38 glucuronidation

44. Reference gene selection for head and neck squamous cell carcinoma gene expression studies

45. Clinical relevance of nine transcriptional molecular markers for the diagnosis of head and neck squamous cell carcinoma in tissue and saliva rinse

47. Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations

48. Management of infertility in a patient presenting with ovarian dysfunction and McCune-Albright syndrome

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