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BERNARD ALTER, MD
MD
Surgery Physician
NPI: 1497817696Individual
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
139812(NY)
Research & Publications (20)
Dyskeratosis congenita: the first NIH clinical research workshop.
PMID 19415736·Pediatr Blood Cancer·2009
8-other
Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia.
PMID 18028488·Br J Haematol·2008
4-observational
Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference.
PMID 18671700·Br J Haematol·2008
8-other
Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry.
PMID 18322251·Haematologica·2008
8-other
Bone marrow cell cycle markers in inherited bone marrow failure syndromes.
PMID 18606449·Leuk Res·2008
8-other
TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita.
PMID 18252230·Am J Hum Genet·2008
8-other
All in the family: disclosure of "unwanted" information to an adolescent to benefit a relative.
PMID 18831063·Am J Med Genet A·2008
5-case
Diagnosis, genetics, and management of inherited bone marrow failure syndromes.
PMID 18024606·Hematology Am Soc Hematol Educ Program·2007
6-review
Metabotropic glutamate receptor 5 modulates nociceptive plasticity via extracellular signal-regulated kinase-Kv4.2 signaling in spinal cord dorsal horn neurons.
PMID 18045912·J Neurosci·2007
7-preclinical
Splenic peliosis and rupture in patients with dyskeratosis congenita on androgens and granulocyte colony-stimulating factor.
PMID 17760812·Br J Haematol·2007
5-case
Endocrine abnormalities in patients with Fanconi anemia.
PMID 17426088·J Clin Endocrinol Metab·2007
8-other
Current diagnosis of inherited bone marrow failure syndromes.
PMID 17454774·Pediatr Hematol Oncol·2007
6-review
Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita.
PMID 17468339·Blood·2007
3-trial
Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.
PMID 16825431·J Med Genet·2007
8-other
Experiences of siblings of patients with Fanconi anemia.
PMID 16779804·Pediatr Blood Cancer·2007
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 532 NEPTUNE AVENUE, SUITE #209
BROOKLYN, NY 11224 - Phone
- (718) 449-8860
Quick Facts
- NPI
- 1497817696
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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