Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
about
Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the LiteratureSeizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.
P2860
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
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2017年學術文章
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2017年學術文章
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name
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
@en
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
@nl
type
label
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
@en
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
@nl
prefLabel
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
@en
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
@nl
P2093
P2860
P50
P356
P1476
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
@en
P2093
Armando Cama
Bruno Nobili
Dominique Vidaud
Giulio Piluso
Giuseppe Cinalli
Giuseppe Mirone
Manoelle Kossorotoff
Michel Zerah
Raphael Calmon
Teresa Giugliano
P2860
P304
P356
10.1002/AJMG.A.38212
P407
P50
P577
2017-04-19T00:00:00Z