Professor, Pediatrics, University of Louisville School of Medicine
Pediatrics
Dr. Alexander Asamoah, MD
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Dr. Alexander Asamoah practices Pediatrics. He went to medical school at University of Ghana Medical School. He received awards:"Fellow", "Nortei-Ababio Prize in Pediatrics", "Bank of Ghana Scholarship (Nominated)" and "Fellow (FAAP)". Alexander Asamoah is a published MD as well. He has 21 publications published. The latest was: A case of insertional translocation involving chromosomes 2 and 4. Alexander Asamoah is registered with Medicare.
Publications
- Molecular characterization of distal 4q duplication in two patients using oligonucleotide array-based comparative genomic hybridization (oaCGH) analysis.
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay.
- Memory and learning in children with 22q11.2 deletion syndrome: evidence for ventral and dorsal stream disruption?
- The neuropsychological phenotype of velocardiofacial syndrome (VCFS): relationship to psychopathology.
- Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.
- Perinatal autopsy findings in three cases of jugular lymphatic obstruction sequence and cardiac polyvalvular dysplasia.
- Identification of ectodysplasin-A receptor gene deletion at 2q12.2 and a potential autosomal MR locus.
- Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.
- Fetal alcohol spectrum disorders (FASD): what medical professionals need to know.
- A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
- Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations.
- Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.
- Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2.
- A case of insertional translocation involving chromosomes 2 and 4.
- Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.
- A major gene model for the familial aggregation of plasma IgA concentration.
- Congenital chylothorax in neonatal thyrotoxicosis.
- 17q inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type one.
- Spontaneous corneal rupture in Noonan syndrome. A case report.
- A deletion in the angiotensin converting enzyme (ACE) gene is common among African Americans with essential hypertension.
Schools
University Of Ghana Medical School Korle Bu
KorleBu Teaching Hospital Accra
Columbia University College Of Physicians and Surgeons
Harvard School Of Medicine
Doctors Specialties
- Clinical Genetics
- Pediatrics
Accepted Insurances
Awards
- Fellow
- Nortei-Ababio Prize in Pediatrics
- Bank of Ghana Scholarship (Nominated)
- Fellow (FAAP)
Education
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Boston Children's Hospital -
Harlem Hospital Center -
University of Ghana Medical School
Hospital
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Norton Hospital -
Kosair Children's Hospital
Drug Facts
| NPI NUMBER | 1639153174 | |
| NPPES Provider LastName | ASAMOAH | |
| NPPES Provider FirstName | ALEXANDER | |
| NPPES Provider ZIPCode | 402021821 | |
| NPPES Provider State | KY | |
| Specialty Description | Pediatric Medicine | |
| Total Claim Count | 74.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1639153174 |
| Last Name Of The Provider | ASAMOAH |
| First Name Of The Provider | ALEXANDER |
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