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JENNY PARMA, D.O.
D.O.
Internal Medicine Physician
NPI: 1285055210IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
20A13834(CA)
CMS Specialties
PrimaryOSTEOPATHIC MANIPULATIVE MEDICINE
Education
OTHER
Class of 2013
Research & Publications (20)
Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 gene.
PMID 18957494·J Clin Endocrinol Metab·2009
5-case
Pseudodominant inheritance of goitrous congenital hypothyroidism caused by TPO mutations: molecular and in silico studies.
PMID 18029453·J Clin Endocrinol Metab·2008
8-other
Rapid and easy prenatal diagnosis of sickle cell anemia using double-dye LNA probe technology.
PMID 17233849·Br J Haematol·2007
8-other
Nephrogenic syndrome of inappropriate antidiuresis in adults: high phenotypic variability in men and women from a large pedigree.
PMID 17229917·J Am Soc Nephrol·2007
8-other
Prenatal diagnosis of primary microcephaly in two consanguineous families by confrontation of morphometry with DNA data.
PMID 16532515·Prenat Diagn·2006
8-other
Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension.
PMID 16429395·Hum Mutat·2006
8-other
GCMB mutation in familial isolated hypoparathyroidism with residual secretion of parathyroid hormone.
PMID 15728199·J Clin Endocrinol Metab·2005
8-other
Prevalence of germline mutations in the TSH receptor gene as a cause of juvenile thyrotoxicosis.
PMID 15384882·Acta Paediatr·2004
8-other
Characterization of a novel loss of function mutation of PAX8 in a familial case of congenital hypothyroidism with in-place, normal-sized thyroid.
PMID 15356023·J Clin Endocrinol Metab·2004
8-other
A novel mutation of tumor necrosis factor receptor alpha type 1 associated with TRAPS and amyloidosis.
PMID 15216558·Am J Med Genet A·2004
8-other
Predictive factors for pancreatic cancer in patients with chronic pancreatitis in association with K-ras gene mutation.
PMID 15202051·Endoscopy·2004
8-other
Thyrotoxic adenoma followed by atypical hyperthyroidism due to struma ovarii: clinical and genetic studies.
PMID 15080771·Eur J Endocrinol·2004
5-case
Serotonin 5-HT(2B) receptor loss of function mutation in a patient with fenfluramine-associated primary pulmonary hypertension.
PMID 14659797·Cardiovasc Res·2003
7-preclinical
Single-nucleotide polymorphism genotyping by melting analysis of dual-labeled probes: examples using factor V Leiden and prothrombin 20210A mutations.
PMID 14500596·Clin Chem·2003
8-other
Oncogenic mutations in the thyrotropin receptor of autonomously functioning thyroid nodules in the Japanese population.
PMID 12213664·Eur J Endocrinol·2002
8-other
A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene.
PMID 11716047·Thyroid·2001
5-case
[Prevention of hemoglobinopathies in Brussels: a necessity?].
PMID 11488080·Rev Med Brux·2001
6-review
Mutation analysis of the Epac--Rap1 signaling pathway in cold thyroid follicular adenomas.
PMID 11375794·Eur J Endocrinol·2001
8-other
A rare variant, I852M, of the RET proto-oncogene in a patient with medullary thyroid carcinoma at age 20 years.
PMID 11295841·Hum Mutat·2001
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
- 1411 E 31ST ST
OAKLAND, CA 94602 - Phone
- (510) 437-8400
Quick Facts
- NPI
- 1285055210
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 20
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