Page 112 - MemoriaER-Eng
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RESEARCH GROUPS







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PROGRAMME:
Group U722
Mitochondrial Medicine





òLead Researcher

Cardellach López, Francesc

Group Members


Contact:
STAFF MEMBERS
Garrabou Tornos, Glria 
Hospital Clinic de Barcelona (HCB) 
Contact: Glria Garrabou / Constanza Morén Morn Nez, Constanza*
c/ Villarroel, 170. Barcelona · Phone: (+34) 93 227 54 00 
ASSOCIATED MEMBERS
E.mail: [email protected] Grau Junyent, Josep Ma
http://www.idibaps.org/recerca/704/recerca-muscular-i-funcio-mitocondrial



Main lines of research


• Creation of the Group for Medical Assistance of Adult Patients with Rare 

Diseases (basically of metabolic and mitochondrial origen, among others).

• Mitochondrial Pathology: Mitochondrial basis of disease and cell processes.

• Muscular Pathology (mitochondrial, inflammatory, autoinmune and toxic).

• Toxicity induced by drugs that cause clinic manifestations of mitochondrial 

origen (Lipodystrophy, hyperlactatemia, peripheral neuropathy, infertility, 
obstetric problems, miopathy.)
13
20
• T 
Toxicity induced by tobacco and carbon monoxide that cause clinic manifes- R
tations of mitochondrial origen.
PO
E
• Mitochondrial basis of Parkinson disease associated to mutations in Parkin L R
A
and LRRK2 genes (rare forms of the disease).
NU
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• Mitochondrial basis of body inclusion myositis.  A
 /
• Mitochondrial function in the study of gene therapy in MNGIE. ER
ER
• Mitochondrial implication in X-Fragile Syndrome. B
CI
• Mitochondrial basis on intrauterine growth restriction.

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* At the expense of Project







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