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WENDEL FRIEDL, MD

MD

Internal Medicine Physician

NPI: 1700832797IndividualAccepts Medicare

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

24159(WI)

CMS Specialties

PrimaryINTERNAL MEDICINE

Education

OHIO STATE UNIVERSITY COLLEGE OF MEDICINE

Class of 1976

Research & Publications (20)

Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers.
PMID 12136244·Hum Genet·2002
8-other
[Experimental examination for optimized stabilisation of trochanteric femur fractures, intra- or extramedullary implant localisation and influence of femur neck component profile on cut-out risk].
PMID 11766660·Chirurg·2001
4-observational
Analysis of rare APC variants at the mRNA level: six pathogenic mutations and literature review.
PMID 19196998·J Mol Diagn·2009
6-review
Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome.
PMID 17973250·J Pathol·2008
8-other
Guidelines for the clinical management of familial adenomatous polyposis (FAP).
PMID 18194984·Gut·2008
6-review
Compound heterozygosity for two MSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus.
PMID 18409202·Am J Med Genet A·2008
5-case
Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families.
PMID 18619730·Cancer Lett·2008
8-other
Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).
PMID 17327285·J Med Genet·2007
6-review
A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification.
PMID 17251345·J Mol Diagn·2007
5-case
High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome.
PMID 17873119·J Med Genet·2007
8-other
Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP).
PMID 17486639·Hum Mutat·2007
8-other
May the APC gene somatic mutations in tumor tissues influence the clinical features of Chinese sporadic colorectal cancers?
PMID 17653897·Acta Oncol·2007
8-other
Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome.
PMID 17653898·Acta Oncol·2007
8-other
MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?
PMID 17199584·Br J Dermatol·2007
5-case
MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype.
PMID 16557584·Int J Cancer·2006
8-other
[Intramedullary locked fixation and compression nail (IP-XS-Nail): treatment of ankle joint fractures].
PMID 16820987·Oper Orthop Traumatol·2006
3-trial
Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer.
PMID 16832876·Cancer Lett·2006
4-observational
[Fracture of the neck of the talus in a child].
PMID 16944078·Unfallchirurg·2006
5-case
Intramedullary locking compression nail for the treatment of an olecranon fracture.
PMID 16953346·Oper Orthop Traumatol·2006
3-trial
Frequency of hereditary non-polyposis colorectal cancer among unselected patients with colorectal cancer in Germany.
PMID 17095871·Digestion·2006
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
6308 8TH AVENUE, SUITE 2000
KENOSHA, WI 53143

Location

Practice Location

6308 8TH AVENUE, KENOSHA, WI
(262) 653-5300

Quick Facts

NPI
1700832797
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
50
Publications
20

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