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DAVID KRAKOW, MD
MD
Hospitalist Physician
NPI: 1295754083IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hospitalist PhysicianPrimary
Hospitalist
Code: 208M00000X
57875(GA)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
UNIVERSITY OF MIAMI, LM MILLER SCHOOL OF MEDICINE
Class of 1999
Research & Publications (20)
The Erlenmeyer flask bone deformity in the skeletal dysplasias.
PMID 19444897·Am J Med Genet A·2009
6-review
Mutations in the gene encoding the calcium-permeable ion channel TRPV4 produce spondylometaphyseal dysplasia, Kozlowski type and metatropic dysplasia.
PMID 19232556·Am J Hum Genet·2009
8-other
Guidelines for the prenatal diagnosis of fetal skeletal dysplasias.
PMID 19265753·Genet Med·2009
7-preclinical
Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene.
PMID 19085972·Prenat Diagn·2009
5-case
Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome.
PMID 19361615·Am J Hum Genet·2009
8-other
A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C-type lectin domain of aggrecan.
PMID 19110214·Am J Hum Genet·2009
8-other
ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulation.
PMID 18677313·Nat Genet·2008
8-other
Expanded clinical spectrum of spondylocarpotarsal synostosis syndrome and possible manifestation in a heterozygous father.
PMID 18257094·Am J Med Genet A·2008
5-case
Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome.
PMID 17635842·Hum Mol Genet·2008
7-preclinical
Spondylocarpotarsal synostosis: long-term follow-up of a case due to FLNB mutations.
PMID 18386804·Am J Med Genet A·2008
5-case
Sprouty 2 disturbs FGFR3 degradation in thanatophoric dysplasia type II: a severe form of human achondroplasia.
PMID 18485666·Cell Signal·2008
7-preclinical
Evaluation of prenatal-onset osteochondrodysplasias by ultrasonography: a retrospective and prospective analysis.
PMID 18627037·Am J Med Genet A·2008
8-other
Type XXVII collagen at the transition of cartilage to bone during skeletogenesis.
PMID 17693149·Bone·2007
7-preclinical
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.
PMID 17078022·Hum Mutat·2007
6-review
Fibroblast growth factors 1, 2, 17, and 19 are the predominant FGF ligands expressed in human fetal growth plate cartilage.
PMID 17314681·Pediatr Res·2007
7-preclinical
Angulated femurs and the skeletal dysplasias: experience of the International Skeletal Dysplasia Registry (1988-2006).
PMID 17486589·Am J Med Genet A·2007
8-other
Cartilage-selective genes identified in genome-scale analysis of non-cartilage and cartilage gene expression.
PMID 17565682·BMC Genomics·2007
4-observational
The skeletal dysplasias: clinical-molecular correlations.
PMID 18056050·Ann N Y Acad Sci·2007
6-review
A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.
PMID 16801345·J Med Genet·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1364 CLIFTON RD NE
ATLANTA, GA 30322 - Phone
- (404) 778-5334
Quick Facts
- NPI
- 1295754083
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 27
- Publications
- 20
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