Overview
Shengju Hao practices practicing medicine in Lanzhou, China.
Hao is highly rated in 4 conditions, according to our data. Their clinical expertise encompasses Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Methylmalonic Acidemia, and Carnitine-Acylcarnitine Translocase Deficiency.
They are actively involved in clinical research, co-authoring 46 peer reviewed articles.
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.
Frequently Asked Questions about Shengju J. Hao
Is Shengju J. Hao a top-rated expert for Maternal Hyperphenylalaninemia?
MediFind is an objective health platform that identifies experts based on real-world data. Shengju J. Hao is classified as an Distinguished expert for Maternal Hyperphenylalaninemia, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Shengju J. Hao participate in research or clinical trials?
Yes. Shengju J. Hao has published 46 articles and abstracts on conditions like Maternal Hyperphenylalaninemia. You can view a list of Shengju J. Hao's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- Maternal Hyperphenylalaninemia
- Advanced
- Carnitine-Acylcarnitine Translocase Deficiency
- Methylmalonic Acidemia
- Phenylketonuria (PKU)
- Experienced
- Acrofacial Dysostosis Rodriguez Type
- Acrofrontofacionasal Dysostosis Syndrome
- Acrokeratoelastoidosis of Costa
- AlbinismHao isExperienced. Learn about Albinism.
- AniridiaHao isExperienced. Learn about Aniridia.
- Aplasia Cutis CongenitaHao isExperienced. Learn about Aplasia Cutis Congenita.
- Benign Essential Blepharospasm
- Brachydactyly Mononen Type
- ChondrodystrophyHao isExperienced. Learn about Chondrodystrophy.
- Clouston SyndromeHao isExperienced. Learn about Clouston Syndrome.
- Cornelia De Lange Syndrome
- Crouzon SyndromeHao isExperienced. Learn about Crouzon Syndrome.
- Delayed GrowthHao isExperienced. Learn about Delayed Growth.
- Dystrophic Epidermolysis Bullosa
- Ectodermal DysplasiasHao isExperienced. Learn about Ectodermal Dysplasias.
- Fukuyama Type Muscular Dystrophy
- Hearing LossHao isExperienced. Learn about Hearing Loss.
- Hermansky-Pudlak SyndromeHao isExperienced. Learn about Hermansky-Pudlak Syndrome.
- HomocystinuriaHao isExperienced. Learn about Homocystinuria.
- HyperventilationHao isExperienced. Learn about Hyperventilation.
- Hypohidrotic Ectodermal Dysplasia
- LissencephalyHao isExperienced. Learn about Lissencephaly.
- Magnesium DeficiencyHao isExperienced. Learn about Magnesium Deficiency.
- Maple Syrup Urine DiseaseHao isExperienced. Learn about Maple Syrup Urine Disease.
- MosaicismHao isExperienced. Learn about Mosaicism.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Oculocutaneous AlbinismHao isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1
- Oculocutaneous Albinism Type 2
- Palmoplantar KeratodermaHao isExperienced. Learn about Palmoplantar Keratoderma.
- Pendred SyndromeHao isExperienced. Learn about Pendred Syndrome.
- Pitt-Hopkins SyndromeHao isExperienced. Learn about Pitt-Hopkins Syndrome.
- Protein DeficiencyHao isExperienced. Learn about Protein Deficiency.
- Retinopathy Pigmentary Mental Retardation
- Russell-Silver DwarfismHao isExperienced. Learn about Russell-Silver Dwarfism.
- Schwartz-Jampel SyndromeHao isExperienced. Learn about Schwartz-Jampel Syndrome.
- Secondary ParkinsonismHao isExperienced. Learn about Secondary Parkinsonism.
- Treacher Collins SyndromeHao isExperienced. Learn about Treacher Collins Syndrome.
- Urea Cycle Disorders (UCD)
- Usher SyndromeHao isExperienced. Learn about Usher Syndrome.
- Walker-Warburg SyndromeHao isExperienced. Learn about Walker-Warburg Syndrome.
- X-Linked Retinal Dysplasia
- X-Linked Spondyloepiphyseal Dysplasia Tarda