Amine Chakroun Selected Research

Pierre Robin syndrome with fetal chondrodysplasia

8/2015

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

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Amine Chakroun Research Topics

Disease

3	Neoplasms (Cancer) 01/2015 - 05/2013
3	Head and Neck Neoplasms (Head and Neck Cancer) 01/2014 - 05/2013
2	Hemorrhage 04/2022 - 01/2017
1	Otosclerosis 01/2020
1	Hearing Loss (Hearing Impairment) 01/2020
1	Pulmonary Embolism 01/2017
1	Pierre Robin syndrome with fetal chondrodysplasia 08/2015
1	Megaepiphyseal dwarfism 08/2015
1	type 3 Stickler syndrome 08/2015
1	Nasal Polyps (Nasal Polyp) 01/2015

Drug/Important Bio-Agent (IBA)

2	Heavy MetalsIBA 01/2015 - 05/2013
2	Cytochrome P-450 CYP2D6 (CYP2D6)IBA 09/2014 - 01/2014
2	ChromiumIBA 11/2013 - 05/2013
2	NickelIBA 11/2013 - 05/2013
1	Tranexamic Acid (AMCA)FDA Link 04/2022
1	OsteoprotegerinIBA 01/2020
1	Capsules (Microcapsules)IBA 01/2020
1	Heparin (Liquaemin)FDA LinkGeneric 01/2017
1	Collagen Type XIIBA 08/2015
1	SuperantigensIBA 01/2015
1	AllergensIBA 01/2015
1	Cytochrome P-450 CYP1A1 (CYP1A1)IBA 01/2014
1	EnzymesIBA 01/2014
1	CadmiumIBA 05/2013
1	MetalsIBA 05/2013
1	ArsenicIBA 05/2013

Therapy/Procedure

1	Thrombectomy 01/2017
1	Conservative Treatment 01/2017
1	Thoracotomy 01/2015