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HARVEY MANDEL, M.D.
M.D.
Ophthalmology Physician
NPI: 1427154293Individual
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
098106(NY)
Research & Publications (20)
A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variability.
PMID 19308961·Am J Med Genet B Neuropsychiatr Genet·2010
8-other
Early treatment with alglucosidase alpha prolongs long-term survival of infants with Pompe disease.
PMID 19542901·Pediatr Res·2009
2-rct
Molecular investigations to improve diagnostic accuracy in patients with ARC syndrome.
PMID 18853461·Hum Mutat·2009
5-case
Familial leukoencephalopathy with slowly progressive dystonia and ataxia.
PMID 19071044·Eur J Paediatr Neurol·2009
5-case
Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease.
PMID 19287243·Genet Med·2009
3-trial
Mutated NDUFS6 is the cause of fatal neonatal lactic acidemia in Caucasus Jews.
PMID 19259137·Eur J Hum Genet·2009
5-case
Population screening in a Druze community: the challenge and the reward.
PMID 19092443·Genet Med·2008
8-other
Methods for a prompt and reliable laboratory diagnosis of Pompe disease: report from an international consensus meeting.
PMID 18078773·Mol Genet Metab·2008
8-other
SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4.
PMID 18179883·Am J Hum Genet·2008
8-other
Defective lamellar granule secretion in arthrogryposis, renal dysfunction, and cholestasis syndrome caused by a mutation in VPS33B.
PMID 18347289·Arch Dermatol·2008
5-case
Erythroderma in a patient taking acitretin for plaque psoriasis.
PMID 18459522·J Drugs Dermatol·2008
5-case
Mitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophy.
PMID 18571143·Am J Hum Genet·2008
8-other
Concentric bladder wall thickening due to haemorrhage following suprapubic aspiration: ultrasound and CT features.
PMID 17684070·Br J Radiol·2007
5-case
The significance of isolated elevation of serum aminotransferases in infants and young children.
PMID 17652319·Arch Dis Child·2007
8-other
Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe disease.
PMID 17151339·Neurology·2007
4-observational
Safe and efficacious allogeneic bone marrow transplantation for nonmalignant disorders using partial T cell depletion and no posttransplantation graft-versus-host-disease prophylaxis.
PMID 17317586·Biol Blood Marrow Transplant·2007
8-other
Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency: a newly recognized association.
PMID 17517257·J Pediatr·2007
5-case
Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapy.
PMID 17999356·Am J Hum Genet·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3725 HENRY HUDSON PKWY
BRONX, NY 10463 - Phone
- (718) 796-9600
Quick Facts
- NPI
- 1427154293
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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