The authors measured coenzyme Q10 (CoQ10) concentration in muscle biopsies from 135 patients with genetically undefined cerebellar ataxia. Thirteen patients with childhood-onset ataxia and cerebellar atrophy had markedly decreased levels of CoQ10. Associated symptoms included seizures, developmental delay, mental retardation, and pyramidal signs. These findings confirm the existence of an ataxic presentation of CoQ10 deficiency, which may be responsive to CoQ10 supplementation
COQ4 encodes a protein that organises the multienzyme complex for the synthesis of coenzyme Q(10) (C...
BACKGROUND: Coenzyme Q10 (CoQ10 or ubiquinone) deficiency can be due either to mutations in genes in...
Coenzyme Q (CoQ) is a lipophilic component of the mitochondrial respiratory enzyme chain, which tran...
The authors measured coenzyme Q10 (CoQ10) concentration in muscle biopsies from 135 patients with ge...
Our aim was to report a new case with cerebellar ataxia associated with coenzyme Q10 (CoQ) deficienc...
OBJECTIVE Primary coenzyme Q(10) deficiency represents a clinically heterogeneous condition sugges...
Primary coenzyme Q10 deficiency-7 is caused by homozygous or compound heterozygous mutations in the ...
COQ8A-ataxia is a mitochondrial disease in which a defect in coenzyme Q10 synthesis leads to dysfunc...
Inherited ataxias are heterogeneous disorders affecting both children and adults, with over 40 diffe...
Coenzyme Q10 (CoQ10, or ubiquinone) is an electron carrier of the mitochondrial respiratory chain (e...
Coenzyme Q(10) is a remarkable lipid involved in many cellular processes such as energy production t...
A 31-year-old woman had encephalopathy, growth retardation, infantilism, ataxia, deafness, lactic ac...
A 31-year-old woman had encephalopathy, growth retardation, infantilism, ataxia, deafness, lactic ac...
Coenzyme Q10 (CoQ10) is an essential component of eukaryotic cells and is involved in crucial bioche...
Coenzyme Q (CoQ) is an essential component of the respiratory chain but also participates in other m...
COQ4 encodes a protein that organises the multienzyme complex for the synthesis of coenzyme Q(10) (C...
BACKGROUND: Coenzyme Q10 (CoQ10 or ubiquinone) deficiency can be due either to mutations in genes in...
Coenzyme Q (CoQ) is a lipophilic component of the mitochondrial respiratory enzyme chain, which tran...
The authors measured coenzyme Q10 (CoQ10) concentration in muscle biopsies from 135 patients with ge...
Our aim was to report a new case with cerebellar ataxia associated with coenzyme Q10 (CoQ) deficienc...
OBJECTIVE Primary coenzyme Q(10) deficiency represents a clinically heterogeneous condition sugges...
Primary coenzyme Q10 deficiency-7 is caused by homozygous or compound heterozygous mutations in the ...
COQ8A-ataxia is a mitochondrial disease in which a defect in coenzyme Q10 synthesis leads to dysfunc...
Inherited ataxias are heterogeneous disorders affecting both children and adults, with over 40 diffe...
Coenzyme Q10 (CoQ10, or ubiquinone) is an electron carrier of the mitochondrial respiratory chain (e...
Coenzyme Q(10) is a remarkable lipid involved in many cellular processes such as energy production t...
A 31-year-old woman had encephalopathy, growth retardation, infantilism, ataxia, deafness, lactic ac...
A 31-year-old woman had encephalopathy, growth retardation, infantilism, ataxia, deafness, lactic ac...
Coenzyme Q10 (CoQ10) is an essential component of eukaryotic cells and is involved in crucial bioche...
Coenzyme Q (CoQ) is an essential component of the respiratory chain but also participates in other m...
COQ4 encodes a protein that organises the multienzyme complex for the synthesis of coenzyme Q(10) (C...
BACKGROUND: Coenzyme Q10 (CoQ10 or ubiquinone) deficiency can be due either to mutations in genes in...
Coenzyme Q (CoQ) is a lipophilic component of the mitochondrial respiratory enzyme chain, which tran...