Overview
Xuefan Gu practices in Shanghai, China. Gu is rated as a Distinguished expert by MediFind in the treatment of Glycogen Storage Disease Type 6. Their top areas of expertise are Malonyl-CoA Decarboxylase Deficiency, Methylmalonic Acidemia, Multiple Carboxylase Deficiency, and Glycogen Storage Disease Type 6.
Their clinical research consists of co-authoring 150 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 Glycogen Storage Disease Type 6.
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
- Distinguished
- Acid Sphingomyelinase Deficiency (ASMD)
- Glycogen Storage Disease Type 6
- HomocystinuriaGu isDistinguished. Learn about Homocystinuria.
- Malonyl-CoA Decarboxylase Deficiency
- Methylmalonic AcidemiaGu isDistinguished. Learn about Methylmalonic Acidemia.
- Multiple Carboxylase Deficiency
- Advanced
- AnorchiaGu isAdvanced. Learn about Anorchia.
- Beta-Ketothiolase Deficiency
- Congenital Adrenal Hyperplasia (CAH)
- Congenital Hypothyroidism
- Gaucher DiseaseGu isAdvanced. Learn about Gaucher Disease.
- Gaucher Disease Type 2
- Experienced
- Acanthosis NigricansGu isExperienced. Learn about Acanthosis Nigricans.
- AchondroplasiaGu isExperienced. Learn about Achondroplasia.
- Addison's DiseaseGu isExperienced. Learn about Addison's Disease.
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- Borjeson-Forssman-Lehmann Syndrome
- Brachydactyly Mononen Type