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MARK MELARAGNO, M.D.
M.D.
Anatomic Pathology & Clinical Pathology Physician
NPI: 1558441535Individual
Specialties, Licenses & Credentials
Anatomic Pathology & Clinical Pathology PhysicianPrimary
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
35068228(OH)
Research & Publications (18)
Interrupted aortic arch type B in A patient with cat eye syndrome.
PMID 19629279·Arq Bras Cardiol·2009
5-case
22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype.
PMID 19565140·Arq Bras Cardiol·2009
8-other
Pure duplication 1q41-qter: further delineation of trisomy 1q syndromes.
PMID 18798309·Am J Med Genet A·2008
5-case
Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation.
PMID 18777129·Hum Genet·2008
8-other
Cerebral nocardiosis in a patient with NHL treated with rituximab.
PMID 17696199·Am J Hematol·2007
8-other
Deletion 22q11.2: report of a complex meiotic mechanism of origin.
PMID 17603802·Am J Med Genet A·2007
5-case
Detection of hidden Y mosaicism in Turner's syndrome: importance in the prevention of gonadoblastoma.
PMID 17128558·J Pediatr Endocrinol Metab·2006
8-other
Screening for fragile X syndrome among Brazilian mentally retarded male patients using PCR from buccal cell DNA.
PMID 17117359·Genet Mol Res·2006
8-other
Deletion of 17p13 and LIS1 gene mutation in isolated lissencephaly sequence.
PMID 16814084·Pediatr Neurol·2006
8-other
Hydrocephaly, penoscrotal transposition, and digital anomalies associated with de novo pseudodicentric rearranged chromosome 13 characterized by classical cytogenetic methods and mBAND analysis.
PMID 16691582·Am J Med Genet A·2006
5-case
Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosome.
PMID 16333825·Am J Med Genet A·2006
5-case
Gas6 inhibits apoptosis in vascular smooth muscle: role of Axl kinase and Akt.
PMID 15380678·J Mol Cell Cardiol·2004
7-preclinical
Duplication 4p and deletion 4p (Wolf-Hirschhorn syndrome) due to complementary gametes from a 3:1 segregation of a maternal balanced t(4;13)(p16;q11) translocation.
PMID 15316961·Am J Med Genet A·2004
5-case
GIT1 mediates Src-dependent activation of phospholipase Cgamma by angiotensin II and epidermal growth factor.
PMID 14523024·J Biol Chem·2003
7-preclinical
Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence.
PMID 12439894·Am J Med Genet·2002
5-case
p160 Bcr mediates platelet-derived growth factor activation of extracellular signal-regulated kinase in vascular smooth muscle cells.
PMID 11560856·Circulation·2001
7-preclinical
Clinical and cytogenetic characterisation of a patient with Down syndrome resulting from a 21q22.1-->qter duplication.
PMID 11334012·J Med Genet·2001
5-case
Cyclophilin A is a secreted growth factor induced by oxidative stress.
PMID 11055983·Circ Res·2000
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
- 18101 LORAIN AVE, DEPARTMENT OF PATHOLOGY
CLEVELAND, OH 44111 - Phone
- (216) 476-7108
Quick Facts
- NPI
- 1558441535
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 18
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