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SUSAN HAYFLICK, MD

MD

Clinical Genetics (M.D.) Physician

NPI: 1538174057IndividualAccepts Medicare

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

MD18081(OR)
Clinical Biochemical Genetics Physician

Medical Genetics — Clinical Biochemical Genetics

Code: 207SG0202X

18081(OR)
Clinical Molecular Genetics Physician

Medical Genetics — Clinical Molecular Genetics

Code: 207SG0203X

18081(OR)
Pediatrics Physician

Pediatrics

Code: 208000000X

MD18081(OR)

CMS Specialties

PrimaryPEDIATRIC MEDICINE

Education

PENNSYLVANIA STATE UNIVERSITY COLLEGE OF MEDICINE

Class of 1985

Research & Publications (20)

Neurodegeneration with brain iron accumulation: from genes to pathogenesis.
PMID 17101457·Semin Pediatr Neurol·2006
6-review
Unraveling the Hallervorden-Spatz syndrome: pantothenate kinase-associated neurodegeneration is the name.
PMID 14631201·Curr Opin Pediatr·2003
6-review
Pantothenate kinase-associated neurodegeneration (formerly Hallervorden-Spatz syndrome).
PMID 12614941·J Neurol Sci·2003
6-review
Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.
PMID 12510040·N Engl J Med·2003
8-other
First scientific workshop on Hallervorden-Spatz syndrome: executive summary.
PMID 11579912·Pediatr Neurol·2001
6-review
Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome.
PMID 11551748·Pediatr Neurol·2001
5-case
Dystonia-parkinsonism disease gene discovery: expect surprises.
PMID 19194873·Ann Neurol·2009
8-other
Clinical and genetic delineation of neurodegeneration with brain iron accumulation.
PMID 18981035·J Med Genet·2009
6-review
Neurodegeneration associated with genetic defects in phospholipase A(2).
PMID 18799783·Neurology·2008
8-other
Infantile neuroaxonal dystrophy: what's most important for the diagnosis?
PMID 18359254·Eur J Paediatr Neurol·2008
8-other
T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation.
PMID 18443312·Neurology·2008
4-observational
Deprivation of pantothenic acid elicits a movement disorder and azoospermia in a mouse model of pantothenate kinase-associated neurodegeneration.
PMID 17429753·J Inherit Metab Dis·2007
7-preclinical
Intellectual and adaptive behaviour functioning in pantothenate kinase-associated neurodegeneration.
PMID 17493025·J Intellect Disabil Res·2007
8-other
Mutations in PLA2G6 and the riddle of Schindler disease.
PMID 17209134·J Med Genet·2007
8-other
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
PMID 17128453·Hum Genet·2006
8-other
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
PMID 17128458·Hum Genet·2006
8-other
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
PMID 17128475·Hum Genet·2006
8-other
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
PMID 17128476·Hum Genet·2006
8-other
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
PMID 17128480·Hum Genet·2006
8-other
Gene symbol: PANK2. Disease: pantothenate kinase-associated neurodegeneration (PKAN).
PMID 17128481·Hum Genet·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
3181 SW SAM JACKSON PARK RD
PORTLAND, OR 97239

Location

Practice Location

3181 SW SAM JACKSON PARK RD, PORTLAND, OR
(503) 494-5516

Quick Facts

NPI
1538174057
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
4
Locations
1
Years in Practice
41
Publications
20

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