Bader Alhaddad Selected Research

Liver Failure

11/2020

Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1.

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Bader Alhaddad Research Topics

Disease

3	Cakut 12/2023 - 01/2017
3	Muscle Hypotonia (Hypotonia) 01/2021 - 12/2017
3	Intellectual Disability (Idiocy) 01/2021 - 01/2017
3	Seizures (Absence Seizure) 01/2021 - 01/2017
3	Brain Diseases (Brain Disorder) 01/2019 - 02/2016
3	Lactic Acidosis 01/2017 - 01/2016
2	Ataxia (Dyssynergia) 12/2021 - 01/2019
2	Dystonia (Limb Dystonia) 11/2020 - 12/2016
2	Polydactyly (Polydactylism) 01/2019 - 01/2017
2	Nervous System Diseases (Neurological Disorders) 01/2018 - 01/2017
2	Atrophy 12/2017 - 01/2017
2	Hyperammonemia 12/2017 - 01/2017
2	Hypertrophic Cardiomyopathy (Hypertrophic Obstructive Cardiomyopathy) 12/2017 - 01/2017
2	Hypoglycemia (Reactive Hypoglycemia) 02/2016 - 01/2016
2	Mitochondrial Diseases (Mitochondrial Disease) 01/2016 - 01/2016
1	Neurodevelopmental Disorders 11/2020
1	Liver Failure 11/2020
1	recessive Spastic paraplegia type 5A 01/2020
1	Fever (Fevers) 01/2020
1	Infantile Spasms (West Syndrome) 01/2020
1	Progressive Myoclonic Epilepsies (Progressive Myoclonic Epilepsy) 01/2019
1	Neurodegenerative Diseases (Neurodegenerative Disease) 11/2018
1	Cholestasis 10/2018
1	Acute Liver Failure (Fulminant Hepatic Failure) 10/2018
1	Dilated Cardiomyopathy (Cardiomyopathy, Congestive) 01/2018
1	Neurodegeneration with brain iron accumulation (NBIA) 01/2018
1	Hereditary Spastic Paraplegia 01/2018
1	Sialorrhea 12/2017
1	Microcephaly 12/2017
1	Reinfection 12/2017
1	Failure to Thrive 01/2017
1	Epilepsy (Aura) 01/2017
1	Neutropenia 01/2017
1	Megaloblastic Anemia 01/2017
1	Rhabdomyolysis 02/2016
1	Agenesis of Corpus Callosum 01/2016
1	Cardiomyopathies (Cardiomyopathy) 01/2016
1	Cardiac Sudden Death (Sudden Cardiac Arrest) 01/2016

Drug/Important Bio-Agent (IBA)

3	Proteins (Proteins, Gene)FDA Link 01/2021 - 01/2016
3	EnzymesIBA 11/2020 - 01/2016
2	Transcription Factors (Transcription Factor)IBA 12/2023 - 03/2023
2	Transaminases (Aminotransferases)IBA 11/2020 - 12/2017
2	Coenzyme A (CoA)IBA 01/2019 - 01/2018
2	Nonsense Codon (Nonsense Mutation)IBA 01/2019 - 12/2016
2	IronIBA 01/2018 - 01/2017
2	UridineIBA 01/2017 - 01/2017
1	phosphatidylethanolamineIBA 12/2021
1	purineIBA 11/2020
1	Amino Acyl-tRNA Synthetases (Aminoacyl-tRNA Synthetase)IBA 11/2020
1	GTPase-Activating Proteins (GTPase-Activating Protein)IBA 01/2020
1	Myelin-Associated GlycoproteinIBA 01/2020
1	Voltage-Gated Potassium Channels (Voltage-Gated Potassium Channel)IBA 01/2019
1	Tuberculin (PPD)IBA 01/2019
1	TransferasesIBA 10/2018
1	Ligases (Synthetase)IBA 01/2018
1	LipidsIBA 01/2018
1	PhosphatidylglycerolsIBA 01/2018
1	Mitochondrial DNA (mtDNA)IBA 12/2017
1	ElementsIBA 01/2017
1	NucleotidesIBA 01/2017
1	OligosaccharidesIBA 01/2017
1	pyrimidineIBA 01/2017
1	Pyruvic Acid (Pyruvate)IBA 01/2017
1	Lactic Acid (Lactate)FDA LinkGeneric 01/2017
1	Amino Acids FDA Link 01/2017
1	RNA Splice SitesIBA 01/2017
1	Oroticaciduria 1IBA 01/2017
1	APTIBA 01/2017
1	Histone MethyltransferasesIBA 12/2016
1	Histones (Histone)IBA 12/2016
1	MethyltransferasesIBA 12/2016
1	Lysine (L-Lysine)FDA Link 12/2016
1	ChromatinIBA 12/2016
1	Fatty Acids (Saturated Fatty Acids)IBA 02/2016
1	Glutamate-tRNA LigaseIBA 01/2016
1	Inorganic Pyrophosphatase (Pyrophosphatase, Inorganic)IBA 01/2016

Therapy/Procedure

1	Hearing Aids (Hearing Aid) 12/2017
1	Cochlear Implants (Cochlear Implant) 12/2017