Overview
Noor Muhammad practices in Kohat, Pakistan. Muhammad is rated as an Experienced expert by MediFind in the treatment of Polydactyly. Their top areas of expertise are Bardet-Biedl Syndrome, Hypohidrotic Ectodermal Dysplasia, Aplasia Cutis Congenita, and Clouston Syndrome.
Their clinical research consists of co-authoring 59 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 2 articles in the study of Polydactyly.
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. Experts 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.
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
- Advanced
- Aplasia Cutis CongenitaMuhammad isAdvanced. Learn about Aplasia Cutis Congenita.
- Bardet-Biedl SyndromeMuhammad isAdvanced. Learn about Bardet-Biedl Syndrome.
- BrachyolmiaMuhammad isAdvanced. Learn about Brachyolmia.
- Clouston SyndromeMuhammad isAdvanced. Learn about Clouston Syndrome.
- Ectodermal DysplasiasMuhammad isAdvanced. Learn about Ectodermal Dysplasias.
- Hypohidrotic Ectodermal Dysplasia
- Experienced
- Achalasia Microcephaly SyndromeMuhammad isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acromesomelic DysplasiaMuhammad isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Anophthalmia Plus SyndromeMuhammad isExperienced. Learn about Anophthalmia Plus Syndrome.