Back to Search
DANIEL STERNBERG, M.D.
M.D.
Emergency Medicine Physician
NPI: 1447639562Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
140221(FL)83489(GA)52497(KY)MD472043(PA)294505(NY)0000059133(TN)
Research & Publications (20)
Platelet activation in the postoperative period after lung transplantation.
PMID 18329493·J Thorac Cardiovasc Surg·2008
8-other
Blockade of receptor for advanced glycation end product attenuates pulmonary reperfusion injury in mice.
PMID 19114209·J Thorac Cardiovasc Surg·2008
7-preclinical
The role of signal transducer and activator of transcription factors in leukemogenesis.
PMID 14722044·J Clin Oncol·2004
6-review
Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis.
PMID 14504341·Neurology·2003
4-observational
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.
PMID 11353725·Brain·2001
8-other
Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.
PMID 11335700·Brain·2001
8-other
Treatment of patients with recurrent and primary refractory acute myelogenous leukemia using mitoxantrone and intermediate-dose cytarabine: a pharmacologically based regimen.
PMID 10813714·Cancer·2000
8-other
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes.
PMID 19570891·Am J Physiol Cell Physiol·2009
8-other
Glucocorticoids may trigger attacks in several types of periodic paralysis.
PMID 19201608·Neuromuscul Disord·2009
5-case
Cold-induced disruption of Na+ channel slow inactivation underlies paralysis in highly thermosensitive paramyotonia.
PMID 19221125·J Physiol·2009
8-other
Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians.
PMID 18337100·Neuromuscul Disord·2009
8-other
Dosage effect of a dominant CLCN1 mutation: a novel syndrome.
PMID 18263754·J Child Neurol·2008
5-case
Severe neonatal non-dystrophic myotonia secondary to a novel mutation of the voltage-gated sodium channel (SCN4A) gene.
PMID 18203179·Am J Med Genet A·2008
5-case
THOC5 spliceosome protein: a target for leukaemogenic tyrosine kinases that affects inositol lipid turnover.
PMID 18373705·Br J Haematol·2008
8-other
Neonatal hypotonia can be a sodium channelopathy: recognition of a new phenotype.
PMID 19015492·Neurology·2008
5-case
A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathy.
PMID 18043288·Diagn Mol Pathol·2007
5-case
Postlung transplant survival is equivalent regardless of cytomegalovirus match status.
PMID 17888958·Ann Thorac Surg·2007
8-other
The oncoprotein NPM-ALK of anaplastic large-cell lymphoma induces JUNB transcription via ERK1/2 and JunB translation via mTOR signaling.
PMID 17690253·Blood·2007
8-other
Comparative efficacy of repetitive nerve stimulation, exercise, and cold in differentiating myotonic disorders.
PMID 17654559·Muscle Nerve·2007
8-other
Akt shows variable sensitivity to an Hsp90 inhibitor depending on cell context.
PMID 17643429·Exp Cell Res·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
Via practice · 2 locations total
- Address
- 111 E 210TH ST
BRONX, NY 10467 - Phone
- (718) 920-4321
Quick Facts
- NPI
- 1447639562
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 6
- Locations
- 2
- Publications
- 20
Are you this provider?
Claim Your Profile