Overview
Shiyue Mei practices practicing medicine in Zhengzhou, China.
Mei is highly rated in 3 conditions, according to our data. Their clinical expertise encompasses Ring Chromosome 18, Methylmalonic Acidemia, Fructose-1,6-Bisphosphatase Deficiency, and Mycoplasma Pneumonia.
They are actively involved in clinical research, co-authoring 55 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 Shiyue Y. Mei
Is Shiyue Y. Mei a top-rated expert for Ring Chromosome 18?
MediFind is an objective health platform that identifies experts based on real-world data. Shiyue Y. Mei is classified as an Advanced expert for Ring Chromosome 18, 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 Shiyue Y. Mei participate in research or clinical trials?
Yes. Shiyue Y. Mei has published 55 articles and abstracts on conditions like Ring Chromosome 18. You can view a list of Shiyue Y. Mei'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
- Advanced
- Fructose-1,6-Bisphosphatase Deficiency
- Methylmalonic Acidemia
- Ring Chromosome 18Mei isAdvanced. Learn about Ring Chromosome 18.
- Experienced
- Angelman SyndromeMei isExperienced. Learn about Angelman Syndrome.
- Aplasia Cutis CongenitaMei isExperienced. Learn about Aplasia Cutis Congenita.
- Atypical PneumoniaMei isExperienced. Learn about Atypical Pneumonia.
- Bile Duct ObstructionMei isExperienced. Learn about Bile Duct Obstruction.
- CHARGE SyndromeMei isExperienced. Learn about CHARGE Syndrome.
- CholestasisMei isExperienced. Learn about Cholestasis.
- CitrullinemiaMei isExperienced. Learn about Citrullinemia.
- Clouston SyndromeMei isExperienced. Learn about Clouston Syndrome.
- Cornelia De Lange Syndrome
- Cortical DysplasiaMei isExperienced. Learn about Cortical Dysplasia.
- CraniosynostosisMei isExperienced. Learn about Craniosynostosis.
- Ectodermal DysplasiasMei isExperienced. Learn about Ectodermal Dysplasias.
- EpilepsyMei isExperienced. Learn about Epilepsy.
- Generalized Tonic-Clonic Seizure
- HomocystinuriaMei isExperienced. Learn about Homocystinuria.
- Hypohidrotic Ectodermal Dysplasia
- IntersexMei isExperienced. Learn about Intersex.
- Limb-Girdle Muscular Dystrophy
- Low Blood SugarMei isExperienced. Learn about Low Blood Sugar.
- Maple Syrup Urine DiseaseMei isExperienced. Learn about Maple Syrup Urine Disease.
- Metabolic AcidosisMei isExperienced. Learn about Metabolic Acidosis.
- Metopic RidgeMei isExperienced. Learn about Metopic Ridge.
- Movement DisordersMei isExperienced. Learn about Movement Disorders.
- Mucopolysaccharidoses (MPS)
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mycoplasma PneumoniaMei isExperienced. Learn about Mycoplasma Pneumonia.
- Noonan SyndromeMei isExperienced. Learn about Noonan Syndrome.
- Partial Androgen Insensitivity Syndrome (PAIS)
- Patent Foramen OvaleMei isExperienced. Learn about Patent Foramen Ovale.
- PlagiocephalyMei isExperienced. Learn about Plagiocephaly.
- PneumoniaMei isExperienced. Learn about Pneumonia.
- Progressive Familial Intrahepatic Cholestasis Type 1
- RASopathiesMei isExperienced. Learn about RASopathies.
- Retinopathy Pigmentary Mental Retardation
- SeizuresMei isExperienced. Learn about Seizures.
- Shwachman-Diamond Syndrome
- Spinal Muscular Atrophy Type 2
- Spinal Muscular Atrophy Type 3
- Status EpilepticusMei isExperienced. Learn about Status Epilepticus.
- Trisomy 18Mei isExperienced. Learn about Trisomy 18.
- Urea Cycle Disorders (UCD)
- UveitisMei isExperienced. Learn about Uveitis.