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M'hamed Grati Selected Research

Pierre Robin syndrome with fetal chondrodysplasia

8/2015Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53.

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M'hamed Grati Research Topics

Disease

8Deafness (Deaf Mutism)
07/2018 - 10/2006
4Hearing Loss (Hearing Impairment)
04/2017 - 02/2013
2Ototoxicity
10/2015 - 12/2014
2Usher Syndromes (Usher Syndrome)
10/2012 - 07/2011
1Nonsyndromic Deafness
01/2020
1Inflammatory Bowel Diseases (Inflammatory Bowel Disease)
09/2017
1Parkinson Disease (Parkinson's Disease)
09/2017
1Disease Progression
09/2017
1Meniere Disease (Menieres Disease)
04/2017
1Autosomal Recessive 31 Deafness
01/2016
1Suppurative Otitis Media
01/2016
1Megaepiphyseal dwarfism
08/2015
1Pierre Robin syndrome with fetal chondrodysplasia
08/2015
1type 3 Stickler syndrome
08/2015
1Autosomal Recessive 66 Deafness
05/2015
1Muscle Hypotonia (Hypotonia)
01/2015
1Ataxia (Dyssynergia)
01/2015
1Arts syndrome
01/2015

Drug/Important Bio-Agent (IBA)

6Proteins (Proteins, Gene)FDA Link
01/2016 - 10/2006
3Anti-Bacterial Agents (Antibiotics)IBA
01/2016 - 12/2014
2Myosin VIIaIBA
01/2016 - 07/2011
2Adenosine Triphosphate (ATP)IBA
01/2016 - 02/2013
1Muscle Proteins (Muscle Protein)IBA
01/2020
1Ribose-Phosphate Pyrophosphokinase (Phosphoribosyl Pyrophosphate Synthetase)IBA
01/2020
1Phosphoric Diester Hydrolases (Phosphodiesterases)IBA
07/2018
1Neurotransmitter Agents (Neurotransmitter)IBA
09/2017
1CatecholaminesIBA
09/2017
1Ion Channels (Ion Channel)IBA
04/2017
1Receptor Tyrosine Kinase-like Orphan ReceptorsIBA
05/2016
1CationsIBA
05/2016
1Protein Isoforms (Isoforms)IBA
05/2016
1DNA (Deoxyribonucleic Acid)IBA
05/2016
1Collagen Type XIIBA
08/2015
1Uric Acid (Urate)IBA
01/2015
1S-Adenosylmethionine (Ademetionine)IBA
01/2015
1purineIBA
01/2015
1radixinIBA
01/2014
1cyclonite (RDX)IBA
01/2014
1Protein Tyrosine PhosphatasesIBA
01/2014

Therapy/Procedure

1Therapeutics
01/2016