Overview
Lianshu Han practices practicing medicine in Shanghai, China.
Han is highly rated in 12 conditions, according to our data. Their clinical expertise encompasses Methylmalonic Acidemia, Malonyl-CoA Decarboxylase Deficiency, Acid Sphingomyelinase Deficiency (ASMD), and Phenylketonuria (PKU).
They are actively involved in clinical research, co-authoring 82 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 Lianshu Z. Han
Is Lianshu Z. Han a top-rated expert for Methylmalonic Acidemia?
MediFind is an objective health platform that identifies experts based on real-world data. Lianshu Z. Han is classified as an Distinguished expert for Methylmalonic Acidemia, 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 Lianshu Z. Han participate in research or clinical trials?
Yes. Lianshu Z. Han has published 82 articles and abstracts on conditions like Methylmalonic Acidemia. You can view a list of Lianshu Z. Han'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
- Acid Sphingomyelinase Deficiency (ASMD)
- Malonyl-CoA Decarboxylase Deficiency
- Methylmalonic AcidemiaHan isDistinguished. Learn about Methylmalonic Acidemia.
- Advanced
- Beta-Ketothiolase Deficiency
- Congenital Adrenal Hyperplasia (CAH)
- Gaucher Disease Type 2
- HomocystinuriaHan isAdvanced. Learn about Homocystinuria.
- HyperglycerolemiaHan isAdvanced. Learn about Hyperglycerolemia.
- Maternal Hyperphenylalaninemia
- Metabolic AcidosisHan isAdvanced. Learn about Metabolic Acidosis.
- Niemann-Pick Disease
- Phenylketonuria (PKU)
- Experienced
- Addison's DiseaseHan isExperienced. Learn about Addison's Disease.
- Adrenal Insufficiency Pediatric
- Brachydactyly Mononen Type
- Congenital Hemolytic Anemia
- Congenital HypothyroidismHan isExperienced. Learn about Congenital Hypothyroidism.
- Farber LipogranulomatosisHan isExperienced. Learn about Farber Lipogranulomatosis.
- Gaucher DiseaseHan isExperienced. Learn about Gaucher Disease.
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Glutaric Acidemia Type 1Han isExperienced. Learn about Glutaric Acidemia Type 1.
- Glutaric Acidemia Type 2Han isExperienced. Learn about Glutaric Acidemia Type 2.
- Glycogen Storage Disease Type 6
- Hemolytic AnemiaHan isExperienced. Learn about Hemolytic Anemia.
- HistiocytosisHan isExperienced. Learn about Histiocytosis.
- HypogonadismHan isExperienced. Learn about Hypogonadism.
- Hypogonadotropic Hypogonadism
- HypothyroidismHan isExperienced. Learn about Hypothyroidism.
- Inborn Amino Acid Metabolism Disorder
- Increased Head Circumference
- IntersexHan isExperienced. Learn about Intersex.
- Isovaleric AcidemiaHan isExperienced. Learn about Isovaleric Acidemia.
- Kallmann SyndromeHan isExperienced. Learn about Kallmann Syndrome.
- Low Sodium LevelHan isExperienced. Learn about Low Sodium Level.
- Maple Syrup Urine DiseaseHan isExperienced. Learn about Maple Syrup Urine Disease.
- Mucolipidosis 3Han isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Han isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidoses (MPS)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Neonatal HypothyroidismHan isExperienced. Learn about Neonatal Hypothyroidism.
- Newborn Low Blood SugarHan isExperienced. Learn about Newborn Low Blood Sugar.
- Non-Langerhans-Cell Histiocytosis
- Patent Ductus ArteriosusHan isExperienced. Learn about Patent Ductus Arteriosus.
- Prader-Willi SyndromeHan isExperienced. Learn about Prader-Willi Syndrome.
- Premature InfantHan isExperienced. Learn about Premature Infant.
- ReticulohistiocytomaHan isExperienced. Learn about Reticulohistiocytoma.
- Short Stature (Growth Disorders)
- Urea Cycle Disorders (UCD)
- Ventricular Septal Defects
- Vitamin B12 Deficiency Anemia