(Q34325030)

1 August 2017

title

Diagnostic profile of neonatal hypotonia: an 11-year study (English)

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1 August 2017

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Richer LP

1

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1 August 2017

Shevell MI

series ordinal

2

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1 August 2017

Miller SP

series ordinal

3

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1 August 2017

publication date

1 July 2001

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1 August 2017

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1 August 2017

volume

25

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1 August 2017

issue

1

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1 August 2017

page(s)

32-37

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Congenital hypotonia revisited

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

The future of the 'floppy infant': a follow-up study of 133 patients.

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

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7 January 2021

Differential diagnosis of diseases producing hypotonia

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada)

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene.

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

SMN(T) and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): genotype/phenotype correlations with disease severity

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

Neonatal Guillain-Barré syndrome: blocking antibodies transmitted from mother to child.

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

Neonatal Guillain-Barré syndrome

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

Peripheral Neuropathy Caused by Proteolipid Protein Gene Mutations

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

Myelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutation

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

The diagnostic yield of the nerve-muscle skin biopsy in paediatric neurology practice. The Montreal Children's Hospital Neuromuscular Group.

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

Clinical approach to inherited peroxisomal disorders: a series of 27 patients

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https://api.crossref.org/works/10.1016%2FS0887-8994%2801%2900277-6

7 January 2021

10.1016/S0887-8994(01)00277-6

Identifiers

DOI

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1 August 2017

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