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DEAN WIECZOREK, D.O.
D.O.
Family Medicine Physician
NPI: 1730445875Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
OS12920(FL)
Research & Publications (20)
Severe nemaline myopathy associated with consecutive mutations E74D and H75Y on a single ACTA1 allele.
PMID 19553116·Neuromuscul Disord·2009
5-case
An internal domain of beta-tropomyosin increases myofilament Ca(2+) sensitivity.
PMID 19429821·Am J Physiol Heart Circ Physiol·2009
7-preclinical
Microcephaly, microtia, preauricular tags, choanal atresia and developmental delay in three unrelated patients: a mandibulofacial dysostosis distinct from Treacher Collins syndrome.
PMID 19334086·Am J Med Genet A·2009
5-case
Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap.
PMID 19277062·Eur J Hum Genet·2009
8-other
A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome.
PMID 19066619·Eur J Hum Genet·2009
5-case
A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients.
PMID 19471318·Eur J Hum Genet·2009
5-case
Allergic contact dermatitis to acid blue 158 in suture material.
PMID 18759915·Contact Dermatitis·2008
5-case
Use of 2-D DIGE analysis reveals altered phosphorylation in a tropomyosin mutant (Glu54Lys) linked to dilated cardiomyopathy.
PMID 18095372·Proteomics·2008
7-preclinical
Divergent regulation of the sarcomere and the cytoskeleton.
PMID 17951248·J Biol Chem·2008
7-preclinical
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.
PMID 18642388·Hum Mutat·2008
8-other
Biallelic loss of function of the promyelocytic leukaemia zinc finger (PLZF) gene causes severe skeletal defects and genital hypoplasia.
PMID 18611983·J Med Genet·2008
5-case
Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders.
PMID 18252226·Am J Hum Genet·2008
7-preclinical
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome.
PMID 18042262·Clin Genet·2008
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383589·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383588·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383596·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383595·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383594·Hum Genet·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 9939 TEXAS 151 ACCESS RD
SAN ANTONIO, TX 78251 - Phone
- (210) 949-9702
Quick Facts
- NPI
- 1730445875
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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