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Autor:
Malandrini A 1, Gabelli S 1, Muglia M 2, Berti G1, Patitucci A2, Sugie K3, Umehara F 5, Quattrone A 2-4, Dotti MT1, Federico A1
Publikováno v:
Neurology 65 (2005): 776.
info:cnr-pdr/source/autori:Malandrini A 1, Gabelli S 1, Muglia M 2, Berti G1, Patitucci A2, Sugie K3, Umehara F 5, Quattrone A 2-4, Dotti MT1, Federico A1/titolo:Motor sensory neuropathy with minifascicle formation in a woman with normal karyotype/doi:/rivista:Neurology/anno:2005/pagina_da:776/pagina_a:/intervallo_pagine:776/volume:65
info:cnr-pdr/source/autori:Malandrini A 1, Gabelli S 1, Muglia M 2, Berti G1, Patitucci A2, Sugie K3, Umehara F 5, Quattrone A 2-4, Dotti MT1, Federico A1/titolo:Motor sensory neuropathy with minifascicle formation in a woman with normal karyotype/doi:/rivista:Neurology/anno:2005/pagina_da:776/pagina_a:/intervallo_pagine:776/volume:65
Minifascicle neuropathy (MN) is a rare developmental malformation of the peripheral nerve characterized by many small fascicles.1 Two unrelated cases, in which the disorder was associated with 46XY pure gonadal dysgenesis (GD),have been reported. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::bb5b10845b33959814a28836d23ac4a4
https://publications.cnr.it/doc/49919
https://publications.cnr.it/doc/49919