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NEIL BUIST, MD, FRCPE

MD, FRCPE

Pediatrics Physician

NPI: 1467617811Individual

Specialties, Licenses & Credentials

Pediatrics PhysicianPrimary

Pediatrics

Code: 208000000X

07658(OR)

Research & Publications (14)

S-adenosylhomocysteine hydrolase deficiency in a 26-year-old man.
PMID 16736098·J Inherit Metab Dis·2006
5-case
Metabolic evaluation of infantile epilepsy: summary recommendations of the Amalfi Group.
PMID 12597059·J Child Neurol·2002
6-review
Experience of working in an Afghan camp.
PMID 12386062·BMJ·2002
8-other
Scene from the USA: the illogic of mandating screening without also providing for treatment.
PMID 17805992·J Inherit Metab Dis·2007
8-other
Contrasting phenotypes in three patients with novel mutations in mitochondrial tRNA genes.
PMID 15670724·Mol Genet Metab·2005
5-case
Two adult galactosaemia females with normal ovarian function and identical GALT mutations (Q188R/R333G).
PMID 12872845·J Inherit Metab Dis·2003
5-case
Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins.
PMID 12410200·J Pediatr·2002
5-case
Height and cataract.
PMID 11756074·Am J Clin Nutr·2002
8-other
Warfarin therapy does not increase bleeding in patients undergoing heart transplantation.
PMID 11565646·Ann Thorac Surg·2001
8-other
Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening program.
PMID 11350183·Mol Genet Metab·2001
8-other
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.
PMID 11137992·Nat Genet·2001
7-preclinical
Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.
PMID 11047755·Am J Hum Genet·2000
5-case
Novel mutations in 13 probands with galactokinase deficiency.
PMID 10790206·Hum Mutat·2000
8-other
Cardiomyopathy in childhood, mitochondrial dysfunction, and the role of L-carnitine.
PMID 10650319·Am Heart J·2000
6-review

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
8510 SW WHITE PINE LN
PORTLAND, OR 97225

Location

Practice Location

8510 SW WHITE PINE LN, PORTLAND, OR
(503) 292-0628

Quick Facts

NPI
1467617811
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
14

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