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KEVIN FLANIGAN, MD

MD

Internal Medicine Physician

NPI: 1003987587Individual

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

014522(ME)

Research & Publications (20)

A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22.
PMID 19318250·Neuromuscul Disord·2009
5-case
Mutation-specific database and bioinformatics resource for DMD.
PMID 19479959·Hum Mutat·2009
8-other
Utility of cystatin C to monitor renal function in Duchenne muscular dystrophy.
PMID 19623638·Muscle Nerve·2009
8-other
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.
PMID 19181672·Brain·2009
8-other
A mutation in the SEPN1 selenocysteine redefinition element (SRE) reduces selenocysteine incorporation and leads to SEPN1-related myopathy.
PMID 19067361·Hum Mutat·2009
8-other
DMD exon 1 truncating point mutations: amelioration of phenotype by alternative translation initiation in exon 6.
PMID 19206170·Hum Mutat·2009
7-preclinical
A phase I/IItrial of MYO-029 in adult subjects with muscular dystrophy.
PMID 18335515·Ann Neurol·2008
3-trial
Late-onset hereditary axonal neuropathies.
PMID 18495953·Neurology·2008
8-other
Clinical and diagnostic features of delayed hypoxic leukoencephalopathy.
PMID 19196933·J Neuropsychiatry Clin Neurosci·2008
5-case
Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene.
PMID 18504129·Neuromuscul Disord·2008
7-preclinical

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

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1111 N CHINA LAKE BLVD STE 190
RIDGECREST, CA 93555

Quick Facts

NPI
1003987587
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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