Haowei Du Selected Research

Wieacker syndrome

1/2022

Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses.

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Haowei Du Research Topics

Disease

3	Brain Diseases (Brain Disorder) 01/2022 - 01/2020
1	Congenital Myasthenic Syndromes (Myasthenia Gravis, Congenital) 01/2022
1	Wieacker syndrome 01/2022
1	Urinary Incontinence 01/2022
1	Renal Insufficiency (Renal Failure) 01/2022
1	Limb-Girdle Muscular Dystrophies (Limb-Girdle Muscular Dystrophy) 01/2022
1	Osteomyelitis 01/2022
1	Rare Diseases (Rare Disease) 01/2022
1	Type IIB Hereditary Sensory And Autonomic Neuropathy 01/2022
1	Epilepsy (Aura) 01/2022
1	Hyperhidrosis 01/2022
1	Emery-Dreifuss Muscular Dystrophy (Scapuloperoneal Muscular Dystrophy) 10/2021
1	Arthrogryposis 06/2021
1	Triple Negative Breast Neoplasms 01/2021
1	Amelogenesis Imperfecta 01/2021
1	Parkinson Disease (Parkinson's Disease) 10/2020
1	Microcephaly 11/2019

Drug/Important Bio-Agent (IBA)

3	Proteins (Proteins, Gene)FDA Link 01/2022 - 11/2019
1	Pharmaceutical PreparationsIBA 01/2022
1	Glutamine (L-Glutamine)FDA Link 01/2022
1	muskIBA 01/2022
1	emerinIBA 10/2021
1	Troponin T (Troponin T1)IBA 06/2021
1	Sodium Citrate FDA LinkGeneric 01/2021
1	DNA (Deoxyribonucleic Acid)IBA 01/2021
1	NucleotidesIBA 10/2020
1	Neurotransmitter Receptors (Neurotransmitter Receptor)IBA 01/2020
1	Ion Channels (Ion Channel)IBA 01/2020
1	TubulinIBA 11/2019

Therapy/Procedure

1	Surgical Amputation (Amputations) 01/2022