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ERAWATI BAWLE, MD

MD

Clinical Genetics (M.D.) Physician

NPI: 1912944919Individual

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

4301933771(MI)
Pediatrics Physician

Pediatrics

Code: 208000000X

4301033771(MI)

Research & Publications (14)

'The cost and yield of evaluations for developmental delay/mental retardation'.
PMID 18834396·Dev Med Child Neurol·2008
8-other
Heterozygous N-terminal deletion of IkappaBalpha results in functional nuclear factor kappaB haploinsufficiency, ectodermal dysplasia, and immune deficiency.
PMID 17931563·J Allergy Clin Immunol·2007
5-case
Growth spurt hypocalcemia.
PMID 16730614·J Adolesc Health·2006
5-case
The neuropsychological phenotype of velocardiofacial syndrome (VCFS): relationship to psychopathology.
PMID 16307864·Arch Clin Neuropsychol·2006
8-other
Memory and learning in children with 22q11.2 deletion syndrome: evidence for ventral and dorsal stream disruption?
PMID 15823983·Child Neuropsychol·2005
8-other
A syndrome of hypoplastic sinuses, hydrocephalus, bronchiectasis, and hypogammaglobulinemia with functional antibody deficiency in twin girls.
PMID 15984604·Ann Allergy Asthma Immunol·2005
5-case
Transmission of ring chromosome 13 from a mother to daughter with both having a 46,XX, r(13)(p13q34) karyotype.
PMID 15326636·Am J Med Genet A·2004
5-case
D-2-Hydroxyglutaric aciduria with absence of corpus callosum and neonatal intracranial haemorrhage.
PMID 12872850·J Inherit Metab Dis·2003
5-case
Medulloblastoma with adverse reaction to radiation therapy in nijmegen breakage syndrome.
PMID 12621246·J Pediatr Hematol Oncol·2003
5-case
Evaluation of surgical intervention in familial isolated simple ectopia lentis: younger v. older generations.
PMID 12171597·Binocul Vis Strabismus Q·2002
4-observational
Special feature: picture of the month. Bannayan-Ruvalcaba-Riley syndrome.
PMID 11177069·Arch Pediatr Adolesc Med·2001
5-case
Orthopaedic manifestations of Ehlers-Danlos syndrome.
PMID 10906878·Clin Orthop Relat Res·2000
8-other
Analphoid 3qter markers.
PMID 10982967·Am J Med Genet·2000
5-case
Blau syndrome (familial granulomatous arthritis, iritis, and rash) in an african-american family.
PMID 19078446·J Clin Rheumatol·2000
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
3901 BEAUBIEN BLVD,, CHILDREN'S HOSPITAL OF MICHIGAN, DIV OF GENETICS.
DETROIT, MI 48201

Location

Practice Location

3901 BEAUBIEN BLVD,, DETROIT, MI
(313) 745-4513

Quick Facts

NPI
1912944919
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
14

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