Natasha J Brown Selected Research

Snijders Blok-Campeau syndrome

1/2022

Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome.

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Natasha J Brown Research Topics

Disease

2	Neurodevelopmental Disorders 01/2022 - 03/2016
1	Acute Liver Failure (Fulminant Hepatic Failure) 05/2022
1	Snijders Blok-Campeau syndrome 01/2022
1	Intellectual Disability (Idiocy) 01/2022
1	Hemangioma (Angioma) 12/2021
1	Xanthomatosis (Xanthoma) 11/2020
1	Sitosterolemia 11/2020
1	Hypercholesterolemia 11/2020
1	Cardiomyopathies (Cardiomyopathy) 01/2020
1	VLCAD deficiency 12/2019
1	Mitochondrial Diseases (Mitochondrial Disease) 12/2019
1	Absent corpus callosum cataract immunodeficiency 03/2016
1	Autism Spectrum Disorder 04/2007
1	Febrile Seizures (Febrile Seizure) 04/2007
1	Seizures (Absence Seizure) 04/2007
1	Brain Diseases (Brain Disorder) 04/2007

Drug/Important Bio-Agent (IBA)

3	Proteins (Proteins, Gene)FDA Link 01/2022 - 01/2022
1	Complementary DNA (cDNA)IBA 05/2022
1	Glutamine (L-Glutamine)FDA Link 01/2022
1	DNA (Deoxyribonucleic Acid)IBA 12/2021
1	oxidized low density lipoproteinIBA 11/2020
1	LDL CholesterolIBA 11/2020
1	gamma-sitosterol (beta-sitosterol)IBA 11/2020
1	SterolsIBA 11/2020
1	Protein Kinases (Protein Kinase)IBA 01/2020
1	Mitochondrial DNA (mtDNA)IBA 12/2019
1	GlycogenIBA 03/2016
1	Pertussis VaccineIBA 04/2007
1	VaccinesIBA 04/2007
1	Sodium Channels (Sodium Channel)IBA 04/2007

Therapy/Procedure

1	Neonatal Intensive Care 12/2019