Experienced in Carbamoyl Phosphate Synthetase 1 Deficiency
Experienced in Carbamoyl Phosphate Synthetase 1 Deficiency
3401 Civic Center Blvd, Children's Hospital Of Philadelphia - Metabolism, 
Philadelphia, PA 

Overview

Marc Yudkoff is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Yudkoff is rated as an Experienced provider by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. His top areas of expertise are Urea Cycle Disorders (UCD), N-Acetylglutamate Synthase Deficiency, Ornithine Translocase Deficiency, and Maple Syrup Urine Disease.

His clinical research consists of co-authoring 36 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article and participated in 1 clinical trial in the study of Carbamoyl Phosphate Synthetase 1 Deficiency.

Specialties
Medical Genetics
Pediatrics
Developmental and Behavioral Pediatrics
Licenses
Clinical Genetics in PA
Languages Spoken
English
Gender
Male

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

CareFirst
  • HMO
  • POS
  • PPO

Locations

3401 Civic Center Blvd, Children's Hospital Of Philadelphia - Metabolism, Philadelphia, PA 19104

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.


2 Clinical Trials

View 1 Less Clinical Trial
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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 Carbamoyl Phosphate Synthetase 1 Deficiency. His top areas of expertise are Classic Galactosemia, Urea Cycle Disorders (UCD), Galactose Epimerase Deficiency, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).

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.

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