Professor, Pediatrics, Washington University School of Medicine
Medical Genetics
Dr. Dorothy K. Grange, MD
|
|
Give Review
Dr. Dorothy K. Grange works in the field of Medical Genetics. He researched medicine at University of Florida College of Medicine. University of Florida College of Medicine is ranked 43 in research and 78 in primary care medicine Dorothy Grange is a published doctor as well. He has 46 publications published. The latest was: Multigenerational autosomal dominant inheritance of 5p chromosomal deletions. Dorothy K. Grange accepts Medicare payments and is listed with Medicare.gov.
Publications
- Multigenerational autosomal dominant inheritance of 5p chromosomal deletions.
- Electrophysiologic consequences of KATP gain of function in the heart: Conduction abnormalities in Cantu syndrome.
- Prolonged exposure to high and variable phenylalanine levels over the lifetime predicts brain white matter integrity in children with phenylketonuria.
- Overnight Pulse Oximetry for Evaluation of Sleep Apnea among Children with Trisomy 21.
- Fabry disease in infancy and early childhood: a systematic literature review.
- Cantú Syndrome Resulting from Activating Mutation in the KCNJ8 Gene.
- Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes.
- Single-dose, subcutaneous recombinant phenylalanine ammonia lyase conjugated with polyethylene glycol in adult patients with phenylketonuria: an open-label, multicentr...
- Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly.
- Phenylketonuria Scientific Review Conference: State of the science and future research needs.
- Sapropterin dihydrochloride use in pregnant women with phenylketonuria: An interim report of the PKU MOMS sub-registry.
- Scoliosis and vertebral anomalies: Additional abnormal phenotypes associated with chromosome 16p11.2 rearrangement.
- Variability in phenylalanine control predicts IQ and executive abilities in children with phenylketonuria.
- White matter integrity and executive abilities following treatment with tetrahydrobiopterin (BH4) in individuals with phenylketonuria.
- White matter integrity and executive abilities in individuals with phenylketonuria.
- Executive response monitoring and inhibitory control in children with phenylketonuria: effects of expectancy.
- KATP channels and cardiovascular disease: suddenly a syndrome.
- Mutations in ECEL1 cause distal arthrogryposis type 5D.
- Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions.
- Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.
- Complex genomic rearrangement of chromosome 16p13.3 detected by array comparative genomic hybridization in a patient with multiple congenital anomalies, dysmorphic cra...
- Safety of extended treatment with sapropterin dihydrochloride in patients with phenylketonuria: Results of a phase 3b study.
- Tetrahydrobiopterin therapy for phenylketonuria in infants and young children.
- IDH2 mutations in patients with D-2-hydroxyglutaric aciduria.
- De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction.
- Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield.
- Distinct clinical and histopathological presentations of Danon cardiomyopathy in young women.
- Age-related decline in the microstructural integrity of white matter in children with early- and continuously-treated PKU: a DTI study of the corpus callosum.
- Pilocytic astrocytoma in a child with Noonan syndrome.
- Mutations in the GGCX and ABCC6 genes in a family with pseudoxanthoma elasticum-like phenotypes.
- Response monitoring in children with phenylketonuria.
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
- Two new patients with Curry-Jones syndrome with trichoblastoma and medulloblastoma suggest an etiologic role of the sonic hedgehog-patched-GLI pathway.
- Case report: Congenital knee dislocation in a patient with larsen syndrome and a novel filamin B mutation.
- Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes.
- Cantu syndrome in a woman and her two daughters: Further confirmation of autosomal dominant inheritance and review of the cardiac manifestations.
- New cases of Bohring-Opitz syndrome, update, and critical review of the literature.
- Inhibitory control in children with phenylketonuria.
- Severe bilateral panlobular emphysema and pulmonary arterial hypoplasia: unusual manifestations of Menkes disease.
- Trisomy 20q13 --> 20qter in a girl with multiple congenital malformations and a recombinant chromosome 20 inherited from a paternal inversion (20)(p13q13.1): clinic...
- Sialidosis presenting as severe nonimmune fetal hydrops is associated with two novel mutations in lysosomal alpha-neuraminidase.
- LIT1 and H19 methylation defects in isolated hemihyperplasia.
- Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
- Amino acid clearance during acute metabolic decompensation in maple syrup urine disease treated with continuous venovenous hemodialysis with filtration.
- Case report: lethal multiple pterygium syndrome.
Schools
University Of Florida
University Fl College Med
University Wi Med School
National Institute Of Health
Doctors Specialties
- Clinical Genetics
- Medical Biochemical Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- LocalPlus
- Open Access Plus
- Commercial Insurance Company
- CoreSource
- Coventry Health Care of Missouri PPO
- Golden Rule
- Homestate Health Plan
- Choice Care PPO
- Medicaid
- Medicare MCR
- Molina
- MultiPlan PPO
- PHCS Network PPO
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
Education
-
University of Wisconsin -
University of Florida -
University of Florida College of Medicine
Hospital
-
St. Louis Children's Hospital
Drug Facts
| NPI NUMBER | 1801812128 | |
| NPPES Provider LastName | GRANGE | |
| NPPES Provider FirstName | DOROTHY | |
| NPPES Provider ZIPCode | 631101002 | |
| NPPES Provider State | MO | |
| Specialty Description | Pediatric Medicine | |
| Total Claim Count | 38.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1801812128 |
| Last Name Of The Provider | GRANGE |
| First Name Of The Provider | DOROTHY |
| View All |
Similar Doctors
|
|
Dr. Beth A. Kozel, MD
 This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Gary S. Gottesman, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Mona A. Yassin, MB BCH
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Ritu L. Zei, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Brittnea J. Adcock, DO |
|
|
Dr. Alison J. Whelan, MD
This Doctor is OpenDoctor Recommended.
 This doctor has more publications
|
|
|
Dr. Su N. Aung, MD |
|
|
Dr. Rick A. Martin, MD |
|
|
Dr. Matthew A. Broom, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Robert S. Kebler, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Ryan E. Longman, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Saroj N. D'Souza, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. James P. Crane, MD |
|
|
Dr. Jennifer M. Heeley, MD |
|
|
Dr. Diana L. Gray, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Kimberly A. Martin, MD |