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BONNIE DE VRIES, MD
MD
Family Medicine Physician
NPI: 1922242163IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
MD19394(ME)60830957(WA)21756(NH)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
ALBANY MEDICAL COLLEGE OF UNION UNIVERSITY
Class of 2009
Research & Publications (20)
First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.
PMID 19220312·Cephalalgia·2009
7-preclinical
Refining the critical region of the novel 19q13.11 microdeletion syndrome to 750 Kb.
PMID 19487540·J Med Genet·2009
8-other
Transition metal impurities on the bond-centered site in germanium.
PMID 19257601·Phys Rev Lett·2009
8-other
Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
PMID 19578123·Hum Mol Genet·2009
8-other
Sexual dimorphism of high molecular weight adiponectin in cord blood.
PMID 18710474·Clin Endocrinol (Oxf)·2009
4-observational
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
PMID 19372089·J Med Genet·2009
8-other
Autosomal dominant inheritance of cardiac valves anomalies in two families: extended spectrum of left-ventricular outflow tract obstruction.
PMID 19161153·Am J Med Genet A·2009
8-other
Preserving organelle vitality: peroxisomal quality control mechanisms in yeast.
PMID 19538506·FEMS Yeast Res·2009
6-review
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.
PMID 19139306·Arch Neurol·2009
5-case
Genomic microarrays in mental retardation: a practical workflow for diagnostic applications.
PMID 19085936·Hum Mutat·2009
6-review
Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study.
PMID 19388127·Hum Mutat·2009
4-observational
Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
PMID 19557186·PLoS Genet·2009
7-preclinical
Transplacental haemorrhage may explain the intrapartum transmission of HIV. A pilot study uses flow cytometry to quantify maternal red blood cells in infants born vaginally or by caesarean section.
PMID 19133046·Aust N Z J Obstet Gynaecol·2008
8-other
Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiency.
PMID 19006216·Am J Med Genet A·2008
5-case
A clinical and genetic study of the Say/Barber/Biesecker/Young-Simpson type of Ohdo syndrome.
PMID 18798845·Clin Genet·2008
8-other
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
PMID 18784092·N Engl J Med·2008
8-other
A high-density association screen of 155 ion transport genes for involvement with common migraine.
PMID 18676988·Hum Mol Genet·2008
8-other
[Sudden blindness: consider Leber's hereditary optic neuropathy].
PMID 19024058·Ned Tijdschr Geneeskd·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
- 133 PLEASANT ST
BERLIN, NH 03570 - Phone
- (603) 752-2040
Quick Facts
- NPI
- 1922242163
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 17
- Publications
- 20
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