(631) 444- KIDS (5437)
- Specialty:
Subspecialty:
- Pediatrics
Pediatric Genetics
- Title(s):
- Professor,
Department of Pediatrics
Division Chief, Pediatric Genetics
PATRICIA GALVIN-PARTON MD
For Appointments:
(631) 444- KIDS (5437)
ALCOHOL, PREGNANCY (FETAL ALCOHOL SYNDROME)
AUTISM
BIOCHEMICAL GENETICS
BIRTH DEFECTS
CLEFT LIP AND PALATE
CLINICAL GENETICS
CONGENITAL DEFECTS (BIRTH DEFECTS)
CONGENITAL HEART DISEASE
CRANIOSYNOSTOSIS (NEWBORN SKULL DISFIGUREMENT)
CYSTIC FIBROSIS
DOWN SYNDROME
GENETIC COUNSELING (GENETICS)
GENETIC DISORDERS
HYPERLIPIDEMIA (CHOLESTEROL)
INBORN ERRORS OF METABOLISM
INFERTILITY
KIDNEY, CYSTS (POLYCYSTIC KIDNEY DISEASE)
MARFAN SYNDROME
MATERNAL PKU
MCAD
MENTAL RETARDATION
METABOLIC DISORDERS
MISCARRIAGE
MITOCHONDRIAL DISORDERS
MYOPATHY
NEUROFIBROMATOSIS
NEUROLOGICAL DISEASES/DISORDERS
NEUROMUSCULAR DISEASES
NEWBORN SCREENING
PEDIATRIC DEFORMITY
PEDIATRIC METABOLIC DISORDERS
PEDIATRIC NEUROLOGIC DISEASE
PKU
PREGNANCY DRUG DANGERS
PREIMPLANTATION GENETIC DIAGNOSIS
PRENATAL DIAGNOSIS (AMNIOCENTESIS)
PRENATAL DIAGNOSIS (CHLORIONIC VILLOUS SAMPLING-CVS)
SIDS
1199NBF
AETNA
AFFINITY HEALTH PLAN
ANTHEM
BEECH STREET
CIGNA GREAT WEST HEALTHCARE
CIGNA HMO
CIGNA PPO
DEVON
EMPIRE BLUE CHOICE HMO
EMPIRE BLUE CHOICE OTHER PLANS
EMPIRE BLUE CHOICE PPO
EMPIRE BLUE CHOICE SENIOR PLAN
FIDELIS CARE NEW YORK
GHI CBP
GHI HMO
HEALTHFIRST
HIP
ISLAND GROUP ADMINISTRATION
MAGNACARE
MEDICAID
MEDICARE
MULTIPLAN
MULTIPLAN PHCS
MULTIPLAN SAVILITY
NEIGHBORHOOD HEALTH PLAN
NO FAULT
SUFFOLK HEALTH PLAN
UNITED EMPIRE PLAN (NYSHIP)
UNITED HEALTHCARE
UNITED OXFORD FREEDOM PLAN
US FAMILY HEALTH PLAN
VYTRA (except SMART START)
WORKERS COMP
Education & Training
- Degree(s):
- New York Medical College, NY
- Residency:
- Pediatrics, Children's Hospital of Los Angeles, CA
- Fellowship:
-
Medical Genetics, Children's Hospital of Los Angeles, CA
Academic & Other
- Teaching Activity:
- Medical Students, Residents, MiniMedical School
- Year Appointed at
Stony Brook:
- 1991
New York State 5 year Genetic Grant - 2004-2009;
New York State Inherited Metabolic Disease Specalty Center - one of 7 Centers in the State; IMD Center of Excellence - Inherited Metabolic Diseases
McAllister Research Award
Guide to America's Top Pediatricans in Medical Genetics
Clinical Trials
Use of Biopterin in patients with Phenylketonuria. Genotype-Phenotype Correlations in patients with Phenylketonuria.
- Clinical Practice Began:
- 1991
Locations
-
PEDIATRICS
37 RESEARCH WAY,
EAST SETAUKET,
NY 11733-3465.
Ph.: 631-444-KIDS
Fax: 631-444-4339
-
PEDIATRICS
6 TECHNOLOGY DRIVE,
EAST SETAUKET,
NY 11733-4079.
Ph.: 631-444-2790
Fax: 631-444-2761


Selected Publications
1)Galvin-Parton, P., and Hommes, F.A. (1996) Abnormal Oligosaccharide pattern in glycogen storage disease type III. Journal of Inherited Metabolic Disease 19(3):383-4.;
2)Galvin-Parton PA, Chen X, Moxham CM, Malbon CC (1997) Induction of G alpha q-specific antisense RNA in vivo causes increased body mass and hyperadiposity. J Biol Chem 1997 Feb 14; 272(7):4335-41.;
3)Acosta, P.B., Yannicelli, S., Parton, P., et. al., (1998) Nutrient Intake and Growth of Infants with Phenylketonuria undergoing Therapy . J Pediatr Gastroenterol Nutr 1998 Sep;27(3):287-91.;
4)Acosta, P.B., Yannicelli S., Parton, P., et.al., (1999) Plasma Micronutrient Concentrations in Infants Undergoing Therapy for Phenylketonuria. Biol Trace Elem Res. Jan;67(1):75-84.;
5)Acosta, P.B., Yannicelli, S., Parton, P., et.al., (1999) Protein Status of Infants with Phenylketonuria undergoing nutrition management. J Am Coll Nutr. 1999 Apr;18(2):102-7.
6)Hagan DM, Ross AJ, Strachan T, Lynch SA, Ruiz-Perez V, Wang YM, Scambler P, Custard E, Reardon W, Hassan S, Muenke M, Nixon P, Papapetrou C, Winter RM, Edwards Y, Morrison K, Barrow M, Galvin-Parton PA, et. al. (2000) Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene. Am J Hum Genet. 2000 May; 66(5):1504-15.
7)Godil, M.A., Galvin-Parton, P.A., Monte, D., Zerah, M., Purandare, A., Wilson, T.A., (2000) Congenital Nasal Pyriform Aperture Stenosis Associated with Central Diabetes Insipidus. J Pediatr. 2000 Au
Personal Statement
We care for Newborns, Children and Adults with any Inherited Metabolic Disorder or any birth defects in a supportive manner. Our staff is highly skilled in providing information and care regarding these disorders.