Wafaa Eyaid Selected Research

Wafaa Eyaid Research Topics

Disease

3	Seizures (Absence Seizure) 01/2021 - 07/2004
2	Inborn Genetic Diseases (Disease, Hereditary) 01/2023 - 09/2013
2	Congenital Disorders of Glycosylation 01/2023 - 07/2004
2	Propionic Acidemia 10/2021 - 01/2019
2	Methylmalonic acidemia 10/2021 - 01/2019
2	Hyperammonemia 10/2021 - 01/2019
2	Cataract (Cataracts) 01/2019 - 07/2003
2	Inborn Errors Metabolism (Inborn Errors of Metabolism) 01/2019 - 01/2015
2	Microcephaly 01/2018 - 01/2015
2	Quadriplegia (Spastic Quadriplegia) 01/2015 - 06/2013
2	Muscle Hypotonia (Hypotonia) 02/2014 - 07/2004
1	Ophthalmoplegia (External Ophthalmoplegia) 01/2022
1	Mitochondrial Diseases (Mitochondrial Disease) 01/2022
1	Leukoencephalopathies 01/2021
1	Hemophagocytic Lymphohistiocytosis (Hemophagocytic Syndrome) 12/2020
1	Zellweger Syndrome (Zellweger's Syndrome) 01/2019
1	Spastic Paraparesis 01/2019
1	Fatigue 01/2019
1	Learning Disabilities (Learning Disability) 01/2019
1	Phenylketonurias (Phenylketonuria) 01/2019
1	Muscle Weakness 01/2019
1	Atrophy 10/2018
1	Sensorineural Hearing Loss 01/2018
1	VLCAD deficiency 01/2018
1	X-Linked Ichthyosis (Ichthyosis, X Linked) 09/2017
1	Psychotic Disorders (Schizoaffective Disorder) 09/2017
1	Schizophrenia (Dementia Praecox) 09/2017
1	Nervous System Diseases (Neurological Disorders) 01/2017
1	Progressive Bulbar Palsy (Fazio Londe Syndrome) 01/2017
1	Deafness (Deaf Mutism) 01/2017
1	Sphingolipidoses (Sphingolipidosis) 01/2016
1	Epilepsy (Aura) 01/2015
1	Cholestasis 03/2014
1	Liver Failure 03/2014
1	Mitochondrial encephalopathy 09/2013
1	Lactic Acidosis 09/2013
1	Basal Ganglia Diseases (Basal Ganglia Disease) 06/2013
1	biotin-responsive Basal ganglia disease 06/2013
1	syndromic 1 Microphthalmia 05/2010
1	Neoplasms (Cancer) 03/2010
1	Intellectual Disability (Idiocy) 04/2005
1	Hepatomegaly 07/2004
1	Hyperpigmentation 07/2003
1	Hypertelorism 07/2003
1	Capillary Hemangioma 07/2003

Drug/Important Bio-Agent (IBA)

3	Proteins (Proteins, Gene)FDA Link 01/2023 - 01/2018
3	Mitochondrial DNA (mtDNA)IBA 01/2022 - 09/2013
2	LipidsIBA 01/2023 - 07/2004
2	carglumic acid FDA Link 10/2021 - 01/2019
2	DNA (Deoxyribonucleic Acid)IBA 01/2021 - 03/2010
2	Fatty Acids (Saturated Fatty Acids)IBA 01/2019 - 01/2018
2	Lactic Acid (Lactate)FDA LinkGeneric 01/2019 - 02/2014
1	Biomarkers (Surrogate Marker)IBA 10/2021
1	AmmoniaIBA 10/2021
1	N-acetyl glutamate synthetase deficiencyIBA 01/2019
1	Serotonin (5 Hydroxytryptamine)IBA 01/2019
1	Amino-Acid N-Acetyltransferase (N-Acetylglutamate Synthase)IBA 01/2019
1	hexadecanal dehydrogenase (acylating) (fatty acyl-CoA reductase)IBA 01/2019
1	Creatine Kinase (Creatine Phosphokinase)IBA 01/2019
1	Dopamine (Intropin)FDA LinkGeneric 01/2019
1	6-propylchromone-2-carboxylic acid (PCCA)IBA 10/2018
1	Anticonvulsants (Antiepileptic Drugs)IBA 10/2018
1	Long-Chain Acyl-CoA Dehydrogenase (Long-Chain-Acyl-Coenzyme A Dehydrogenase)IBA 01/2018
1	Nonsense Codon (Nonsense Mutation)IBA 01/2018
1	EnzymesIBA 09/2017
1	Steryl-Sulfatase (Steroid Sulfatase)IBA 09/2017
1	Riboflavin (Vitamin B2)FDA LinkGeneric 01/2017
1	Lysergic Acid Diethylamide (LSD)IBA 01/2016
1	Aspartate-Ammonia Ligase (Asparagine Synthetase)IBA 01/2015
1	deoxyguanosine kinaseIBA 03/2014
1	Thiamine (Aneurin)FDA Link 06/2013
1	Biotin (Vitamin H)FDA Link 06/2013
1	beta CateninIBA 05/2010
1	molybdopterin (molybdenum cofactor)IBA 04/2005
1	Sulfite OxidaseIBA 04/2005
1	OligosaccharidesIBA 07/2004

Therapy/Procedure

1	Length of Stay 10/2021
1	Sutures (Suture) 07/2003