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KATHRYN BOYLAN, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1275113961Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Characterization of DCTN1 genetic variability in neurodegeneration.
PMID 19506225·Neurology·2009
8-other
Defining normal duration for afterdischarges with repetitive nerve stimulation: a pilot study.
PMID 19151616·J Clin Neurophysiol·2009
8-other
The severe mood dysregulation phenotype: case description of a female adolescent.
PMID 19018324·J Can Acad Child Adolesc Psychiatry·2008
8-other
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.
PMID 18802454·PLoS Genet·2008
8-other
A novel, efficient, randomized selection trial comparing combinations of drug therapy for ALS.
PMID 18608093·Amyotroph Lateral Scler·2008
3-trial
Motility screen identifies Drosophila IGF-II mRNA-binding protein--zipcode-binding protein acting in oogenesis and synaptogenesis.
PMID 18282112·PLoS Genet·2008
7-preclinical
Efficacy of minocycline in patients with amyotrophic lateral sclerosis: a phase III randomised trial.
PMID 17980667·Lancet Neurol·2007
3-trial
Comorbidity of internalizing disorders in children with oppositional defiant disorder.
PMID 17896121·Eur Child Adolesc Psychiatry·2007
1-meta
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
PMID 17826340·Lancet Neurol·2007
8-other
Review: antidepressants may increase risk of self-harm or suicidal behaviour in children and adolescents.
PMID 17652571·Evid Based Ment Health·2007
8-other
A transgenic mouse model of plasma cell malignancy shows phenotypic, cytogenetic, and gene expression heterogeneity similar to human multiple myeloma.
PMID 17483317·Cancer Res·2007
7-preclinical
Aprataxin (APTX) gene mutations resembling multiple system atrophy.
PMID 17049295·Parkinsonism Relat Disord·2007
5-case
Psychopharmacologic treatment of pediatric major depressive disorder.
PMID 16896960·Psychopharmacology (Berl)·2007
6-review
No evidence that polymorphisms in CYP2C8, CYP2C9, UGT1A6, PPARdelta and PPARgamma act as modifiers of the protective effect of regular NSAID use on the risk of colorectal carcinoma.
PMID 16141797·Pharmacogenet Genomics·2005
4-observational
Impact of comorbid anxiety disorders on outcome in a cohort of patients with bipolar disorder.
PMID 15323597·J Clin Psychiatry·2004
4-observational
Mini-clusters of potentially prodromal symptoms may identify psychiatrically well Amish children at higher risk of developing bipolar I disorder.
PMID 14769670·Evid Based Ment Health·2004
8-other
Association of the Pro12Ala and C1431T variants of PPARG and their haplotypes with susceptibility to Type 2 diabetes.
PMID 14730381·Diabetologia·2004
8-other
Methyl parathion in residential properties: relocation and decontamination methodology.
PMID 12634141·Environ Health Perspect·2002
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 6431 FANNIN ST, MSE R462
HOUSTON, TX 77030 - Phone
- (713) 500-6784
Quick Facts
- NPI
- 1275113961
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 20
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