NS 38181/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

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Subject: NS 38181/NS/NINDS NIH HHS/United States[Grants an - PubMed

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Year	Number of Results
2001	3
2002	1
2025	0

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Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy.

Jeannet PY, Watts GD, Bird TD, Chance PF. Jeannet PY, et al. Neurology. 2001 Dec 11;57(11):1963-8. doi: 10.1212/wnl.57.11.1963. Neurology. 2001. PMID: 11739810

Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy.

Watts GD, O'Briant KC, Borreson TE, Windebank AJ, Chance PF. Watts GD, et al. Neurology. 2001 Mar 13;56(5):675-8. doi: 10.1212/wnl.56.5.675. Neurology. 2001. PMID: 11245726

Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families.

Watts GD, O'Briant KC, Chance PF. Watts GD, et al. Hum Genet. 2002 Feb;110(2):166-72. doi: 10.1007/s00439-001-0647-5. Epub 2001 Dec 18. Hum Genet. 2002. PMID: 11935323

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