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NATALYA NADAL, M.D.
M.D.
Pediatrics Physician
NPI: 1952364846Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
MD00043091(WA)
Research & Publications (14)
Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L gene.
PMID 19508421·Clin Genet·2009
5-case
Prognostic value of CXCR4 and FAK expression in acute myelogenous leukemia.
PMID 19042019·Leuk Res·2009
8-other
Heterogeneous patterns of amplification of the NUP214-ABL1 fusion gene in T-cell acute lymphoblastic leukemia.
PMID 18923437·Leukemia·2009
8-other
Genome profiling of acute myelomonocytic leukemia: alteration of the MYB locus in MYST3-linked cases.
PMID 18818702·Leukemia·2009
8-other
Acute myeloid leukaemia with 8p11 (MYST3) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologique.
PMID 18528428·Leukemia·2008
8-other
Significance of heat-shock protein (HSP) 90 expression in acute myeloid leukemia cells.
PMID 18386162·Cell Stress Chaperones·2008
8-other
RUNX1 rearrangements in acute myeloblastic leukemia relapsing after hematopoietic stem cell transplantation.
PMID 18206548·Cancer Genet Cytogenet·2008
5-case
Multiparametric analysis of normal and postchemotherapy bone marrow: Implication for the detection of leukemia-associated immunophenotypes.
PMID 18061947·Cytometry B Clin Cytom·2008
8-other
Hyperdiploid karyotypes in acute myeloid leukemia define a novel entity: a study of 38 patients from the Groupe Francophone de Cytogenetique Hematologique (GFCH).
PMID 17928884·Leukemia·2008
4-observational
Successful treatment with imatinib mesylate in a case of chronic myeloproliferative disorder with a t(5;12)(q33;p13.1) without eosinophilia.
PMID 16938578·Cancer Genet Cytogenet·2006
5-case
Expression and prognostic significance of heat-shock proteins in myelodysplastic syndromes.
PMID 16670079·Haematologica·2006
8-other
NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique.
PMID 16467868·Leukemia·2006
8-other
Spinocerebellar ataxia type 2 (SCA2) with white matter involvement.
PMID 15896478·Neurosci Lett·2005
5-case
Prenatal diagnosis of a partial trisomy 7q in two fetuses with bilateral ventriculomegaly.
PMID 11113903·Prenat Diagn·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 501 SE 172ND AVE
VANCOUVER, WA 98684 - Phone
- (360) 882-2778
Quick Facts
- NPI
- 1952364846
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 14
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