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BRANDI MENDONCA, MD
MD
Family Medicine Physician
NPI: 1306941869IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
MD26831(OR)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
WARREN ALPERT MEDICAL SCHOOL OF BROWN UNIVERSITY
Class of 2003
Research & Publications (20)
Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene.
PMID 11932321·J Clin Endocrinol Metab·2002
5-case
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1.
PMID 19489874·Clin Endocrinol (Oxf)·2010
5-case
Expression profiles of the glucose-dependent insulinotropic peptide receptor and LHCGR in sporadic adrenocortical tumors.
PMID 18971217·J Endocrinol·2009
4-observational
Analysis of glucose-dependent insulinotropic peptide receptor (GIPR) and luteinizing hormone receptor (LHCGR) expression in human adrenocortical hyperplasia.
PMID 19578593·Arq Bras Endocrinol Metabol·2009
8-other
Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant.
PMID 19036620·Growth Horm IGF Res·2009
4-observational
Analysis of craniofacial and extremity growth in patients with growth hormone deficiency during growth hormone therapy.
PMID 19188743·Horm Res·2009
3-trial
The -202 A allele of insulin-like growth factor binding protein-3 (IGFBP3) promoter polymorphism is associated with higher IGFBP-3 serum levels and better growth response to growth hormone treatment in patients with severe growth hormone deficiency.
PMID 18984657·J Clin Endocrinol Metab·2009
3-trial
Noonan syndrome and related disorders: a review of clinical features and mutations in genes of the RAS/MAPK pathway.
PMID 19258709·Horm Res·2009
6-review
High prevalence of pituitary magnetic resonance abnormalities and gene mutations in a cohort of Brazilian children with growth hormone deficiency and response to treatment.
PMID 18780602·J Pediatr Endocrinol Metab·2008
8-other
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.
PMID 18682503·J Clin Endocrinol Metab·2008
8-other
Expression of insulin-like growth factor-II and its receptor in pediatric and adult adrenocortical tumors.
PMID 18611974·J Clin Endocrinol Metab·2008
4-observational
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family.
PMID 19169480·Arq Bras Endocrinol Metabol·2008
5-case
Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients.
PMID 18331608·Clin Endocrinol (Oxf)·2008
8-other
Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA).
PMID 19169498·Arq Bras Endocrinol Metabol·2008
5-case
Tall stature and poor breast development after estrogen replacement in a hypergonadotrophic hypogonadic patient with a 45,X/46,X,der(X) karyotype with SHOX gene overdosage.
PMID 19169482·Arq Bras Endocrinol Metabol·2008
5-case
Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a homozygous 25 BP duplication (NT 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon predicted by molecular modeling.
PMID 19169487·Arq Bras Endocrinol Metabol·2008
5-case
Factors determining normal adult height in girls with gonadotropin-dependent precocious puberty treated with depot gonadotropin-releasing hormone analogs.
PMID 18460564·J Clin Endocrinol Metab·2008
8-other
[Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with Carney complex caused by the novel nonsense mutation p.Y21X].
PMID 19169478·Arq Bras Endocrinol Metabol·2008
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2163 NW 2ND ST
MCMINNVILLE, OR 97128 - Phone
- (503) 472-4197
Quick Facts
- NPI
- 1306941869
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 23
- Publications
- 20
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