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KENDALL FLANIGAN, MD
MD
Dermatology Physician
NPI: 1679154603IndividualAccepts Medicare
Specialties, Licenses & Credentials
Dermatology PhysicianPrimary
Dermatology
Code: 207N00000X
2025-02105(NC)
CMS Specialties
PrimaryDERMATOLOGY
Education
MEDICAL COLLEGE OF GEORGIA SCHOOL OF MEDICINE
Class of 2021
Research & Publications (20)
A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22.
PMID 19318250·Neuromuscul Disord·2009
5-case
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
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
Factors influencing therapists' interventions for children with learning difficulties.
PMID 18510254·Can J Occup Ther·2008
8-other
Exon skipping mutations in collagen VI are common and are predictive for severity and inheritance.
PMID 18366090·Hum Mutat·2008
8-other
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy.
PMID 18274675·J Clin Invest·2008
8-other
Mitochondrial fusion and function in Charcot-Marie-Tooth type 2A patient fibroblasts with mitofusin 2 mutations.
PMID 18316077·Exp Neurol·2008
8-other
Selenoprotein N is required for ryanodine receptor calcium release channel activity in human and zebrafish muscle.
PMID 18713863·Proc Natl Acad Sci U S A·2008
7-preclinical
DMD pseudoexon mutations: splicing efficiency, phenotype, and potential therapy.
PMID 18059005·Ann Neurol·2008
5-case
Paraneoplastic myopathy: response to intravenous immunoglobulin.
PMID 17336069·Neuromuscul Disord·2007
5-case
Abnormal expression of mu-crystallin in facioscapulohumeral muscular dystrophy.
PMID 17451686·Exp Neurol·2007
8-other
Distinctive patterns of microRNA expression in primary muscular disorders.
PMID 17942673·Proc Natl Acad Sci U S A·2007
8-other
A comparative analysis of collagen VI production in muscle, skin and fibroblasts from 14 Ullrich congenital muscular dystrophy patients with dominant and recessive COL6A mutations.
PMID 16935502·Neuromuscul Disord·2006
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 7903 PROVIDENCE RD STE 125
CHARLOTTE, NC 28277 - Phone
- (704) 727-7355
Quick Facts
- NPI
- 1679154603
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 5
- Publications
- 20
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