M Gribaa Selected Research

Glycogen

12/2012

A c.3216_3217delGA mutation in AGL gene in Tunisian patients with a glycogen storage disease type III: evidence of a founder effect.

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M Gribaa Research Topics

Disease

1	Mucopolysaccharidosis II (Hunter Syndrome) 01/2020
1	Piebaldism (Partial Albinism) 06/2015
1	Glycogen Storage Disease Type III (Cori's Disease) 12/2012
1	Hyperthermia 04/2011
1	Wounds and Injuries (Trauma) 04/2011
1	Self Mutilation 04/2011
1	Fever (Fevers) 04/2011
1	Muscle Hypotonia (Hypotonia) 04/2011
1	Hereditary Sensory and Autonomic Neuropathies (HSAN) 04/2011
1	Ataxia (Dyssynergia) 07/2007
1	Ophthalmoplegia (External Ophthalmoplegia) 07/2007
1	Infantile onset spinocerebellar ataxia 07/2007
1	Sensory Partial Epilepsy 07/2007
1	Dysarthria (Spastic Dysarthria) 07/2007
1	Retinal Dystrophies 04/2004
1	Apraxias (Dyspraxia) 04/2004
1	Coloboma (Colobomas) 04/2004

Drug/Important Bio-Agent (IBA)

1	GlycosaminoglycansIBA 01/2020
1	Iduronic Acid (Iduronate)IBA 01/2020
1	Protein-Tyrosine Kinases (Tyrosine Kinase)IBA 06/2015
1	amylo-1,6-glucosidaseIBA 12/2012
1	GlycogenIBA 12/2012
1	Glycogen Debranching Enzyme System (Glycogen Debranching Enzyme)IBA 12/2012
1	Chlorpromazine (Thorazine)FDA Link 04/2011
1	Histamine (Histamine Dihydrochloride)FDA Link 04/2011
1	AntipyreticsIBA 04/2011
1	Mitochondrial Proteins (Mitochondrial Protein)IBA 07/2007
1	Retinaldehyde (Retinal)IBA 04/2004

Therapy/Procedure

1	Intradermal Injections 04/2011