Overview
Michael Bober is a Medical Genetics specialist and a Pediatrics provider in Wilmington, Delaware. Dr. Bober is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Achondroplasia, Osteotomy, and Adenoidectomy. Dr. Bober is currently accepting new patients.
His clinical research consists of co-authoring 123 peer reviewed articles and participating in 6 clinical trials. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
6 Clinical Trials
Childrens Health Care Associates Inc
Can Ficicioglu is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Ficicioglu is rated as a Distinguished provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Classic Galactosemia, Urea Cycle Disorders (UCD), Galactose Epimerase Deficiency, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
Childrens Health Care Associates Inc
Rebecca Ahrens-Nicklas is a Pediatrics specialist and a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Ahrens-Nicklas is rated as an Elite provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Multiple Sulfatase Deficiency, Cardiomyopathic Lentiginosis, Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, and Noonan Syndrome.
Mary Pipan is a Developmental and Behavioral Pediatrics specialist and a Physiatrist in Philadelphia, Pennsylvania. Dr. Pipan is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Autism Spectrum Disorder, Delayed Growth, Apraxia, Cardiofaciocutaneous Syndrome, and Myringotomy.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Elite
- Achalasia Microcephaly Syndrome
- AchondrogenesisDr. Bober isElite. Learn about Achondrogenesis.
- AchondroplasiaDr. Bober isElite. Learn about Achondroplasia.
- Acromesomelic DysplasiaDr. Bober isElite. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Distinguished
- Acromicric DysplasiaDr. Bober isDistinguished. Learn about Acromicric Dysplasia.
- Chondrodysplasia Punctata SyndromeDr. Bober isDistinguished. Learn about Chondrodysplasia Punctata Syndrome.
- Cortical DysplasiaDr. Bober isDistinguished. Learn about Cortical Dysplasia.
- Diastrophic DysplasiaDr. Bober isDistinguished. Learn about Diastrophic Dysplasia.
- Kozlowski Spondylometaphyseal DysplasiaDr. Bober isDistinguished. Learn about Kozlowski Spondylometaphyseal Dysplasia.
- MicrognathiaDr. Bober isDistinguished. Learn about Micrognathia.
- Advanced
- Atelosteogenesis Type 2Dr. Bober isAdvanced. Learn about Atelosteogenesis Type 2.
- Buschke-Ollendorff SyndromeDr. Bober isAdvanced. Learn about Buschke-Ollendorff Syndrome.
- Cartilage-Hair HypoplasiaDr. Bober isAdvanced. Learn about Cartilage-Hair Hypoplasia.
- Chondrodysplasia, Grebe TypeDr. Bober isAdvanced. Learn about Chondrodysplasia, Grebe Type.
- CHST3-Related Skeletal Dysplasia
- Craniometaphyseal DysplasiaDr. Bober isAdvanced. Learn about Craniometaphyseal Dysplasia.
- Experienced
- 2q37 Deletion SyndromeDr. Bober isExperienced. Learn about 2q37 Deletion Syndrome.
- 3M SyndromeDr. Bober isExperienced. Learn about 3M Syndrome.
- 3MC SyndromeDr. Bober isExperienced. Learn about 3MC Syndrome.
- 47 XYY SyndromeDr. Bober isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Bober isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Bober isExperienced. Learn about Abruzzo-Erickson Syndrome.