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Yolanda Campos

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Henry Rivera; Alberto Blázquez; Julián Carretero; José C Alvarez-Cermeño; Yolanda Campos; Ana Cabello; Emiliano Gonzalez-Vioque; Belén Borstein; Rafael Garesse; Joaquín Arenas; Miguel A Martín
Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicase.
E Maeso; A Rueda; S Jiménez; Pilar del Hoyo; R Martín; Ana Cabello; L M Mendoza; Joaquín Arenas; Yolanda Campos
A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathy.
Emiliano González-Vioque; Alberto Blázquez; Daniel Fernández-Moreira; Belén Bornstein; Juan Bautista; Javier Arpa; Carmen Navarro; Yolanda Campos; Miguel Angel Fernández-Moreno; Rafael Garesse; Joaquín Arenas; Miguel A Martín
Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population.

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2007: Henry Rivera; Alberto Blázquez; Julián Carretero; José C Alvarez-Cermeño; Yolanda Campos; Ana Cabello; Emiliano Gonzalez-Vioque; Belén Borstein; Rafael Garesse; Joaquín Arenas; Miguel A Martín
Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicase.
Neuromuscular disorders : NMD 2007;17(9-10):677-80.
2007: E Maeso; A Rueda; S Jiménez; Pilar del Hoyo; R Martín; Ana Cabello; L M Mendoza; Joaquín Arenas; Yolanda Campos
A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathy.
Neuromuscular disorders : NMD 2007;17(5):415-8.
2006: Emiliano González-Vioque; Alberto Blázquez; Daniel Fernández-Moreira; Belén Bornstein; Juan Bautista; Javier Arpa; Carmen Navarro; Yolanda Campos; Miguel Angel Fernández-Moreno; Rafael Garesse; Joaquín Arenas; Miguel A Martín
Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population.
Archives of neurology 2006;63(1):107-11.
2005: A Blazquez; Miguel A Martín; Maria Carmen Lara; Ramon Martí; Yolanda Campos; Ana Cabello; Rafael Garesse; Juan Bautista; Antoni L Andreu; Joaquín Arenas
Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE.
Neuromuscular disorders : NMD 2005;15(11):775-8.
2005: Elena Martín-Hernández; Maria Teresa García-Silva; Julia Vara; Yolanda Campos; Ana Cabello; Rafael Muley; Pilar del Hoyo; Miguel A Martín; Joaquín Arenas
Renal pathology in children with mitochondrial diseases.
Pediatric nephrology (Berlin, Germany) 2005;20(9):1299-305.
2005: Belén Bornstein; José-Antonio Mas; Clarice Patrono; Miguel Angel Fernández-Moreno; Emiliano González-Vioque; Yolanda Campos; Rosalba Carrozzo; Miguel A Martín; Pilar del Hoyo; Filippo M Santorelli; Joaquín Arenas; Rafael Garesse
Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene.
The Biochemical journal 2005;387(Pt 3):773-8.
2005: Miguel A Martín; Alberto Blázquez; Luis G Gutierrez-Solana; Daniel Fernández-Moreira; Paz Briones; Antoni L Andreu; Rafael Garesse; Yolanda Campos; Joaquín Arenas
Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene.
Archives of neurology 2005;62(4):659-61.
2005: Susana Navarro; Pilar del Hoyo; Yolanda Campos; Marie Abitbol; María-José Morán-Jiménez; María García-Bravo; Pilar Ochoa; Montserrat Grau; Xavier Montagutelli; Jorge Frank; Rafael Garesse; Joaquín Arenas; Rafael Enríquez de Salamanca; Antonio Fontanellas
Increased mitochondrial respiratory chain enzyme activities correlate with minor extent of liver damage in mice suffering from erythropoietic protoporphyria.
Experimental dermatology 2005;14(1):26-33.
2004: Miguel A Martín; Alberto Blázquez; Ramon Martí; Juan Bautista; Maria Carmen Lara; Ana Cabello; Yolanda Campos; O Belda; Antoni L Andreu; Joaquín Arenas
Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIE.
Neurology 2004;63(8):1536-7.
2003: Yolanda Campos; A García; Pilar del Hoyo; P Jara; Miguel A Martín; Juan C Rubio; A Berbel; J R Barberá; Renee Ribacoba; AURORA ASTUDILLO; Ana Cabello; José R Ricoy; Joaquín Arenas
Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypes.
Neuromuscular disorders : NMD 2003;13(5):416-20.
2003: Manuel Seijo-Martínez; María Castro del Río; Yolanda Campos; Francisco Palau; Joaquín Arenas; Susana Teijeira; Roberto Fernández Hojas; Carmen Navarro
Unusual clinical findings and Complex III deficiency in a family with myotonic dystrophy.
Journal of the neurological sciences 2003;208(1-2):87-91.
2003: Rosalba Carrozzo; Belén Bornstein; Simona Lucioli; Yolanda Campos; P de la Pena; N Petit; Carlo Dionisi Vici; Laura Vilarinho; Teresa Rizza; Enrico Bertini; Rafael Garesse; Filippo M Santorelli; Joaquín Arenas
Mutation analysis in 16 patients with mtDNA depletion.
Human mutation 2003;21(4):453-4.
2003: Adelaida García-Velasco; Carlos Gómez-Escalonilla; Juan-Manuel Guerra Vales; Ana Cabello; Yolanda Campos; Joaquín Arenas
Intestinal pseudo-obstruction and urinary retention: cardinal features of a mitochondrial DNA-related disease.
Journal of internal medicine 2003;253(3):381-5.
2003: Joaquín Arenas; Miguel Angel Fernández-Moreno; José Antonio Molina; V Fernández; Pilar del Hoyo; Yolanda Campos; P Calvo; Miguel A Martín; A García; Teresa Moreno; Antonio Martínez-Salio; B Börnstein; Félix Bermejo; Ana Cabello; Rafael Garesse
Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozil.
Neurology 2003;60(1):124-6.
2002: Alberto García-Redondo; F Bustos; B Juan Y Seva; Pilar del Hoyo; S Jiménez; Yolanda Campos; Miguel A Martín; Juan C Rubio; F Cañadillas; Joaquín Arenas; J Esteban
Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis.
Muscle & nerve 2002;26(2):274-8.
2002: Yolanda Campos; Miguel A Martín; Joaquín Arenas
[Molecular genetics of disorders of the mitochondrial respiratory chain].
Revista de neurologia 2002;35(2):153-8.
2002: Belén Bornstein; José-Antonio Mas; Miguel Angel Fernández-Moreno; Yolanda Campos; Miguel A Martín; Pilar del Hoyo; Juan C Rubio; Joaquín Arenas; Rafael Garesse
The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines.
Human mutation 2002;19(3):234-9.
2002: Yolanda Campos; A García; A López; S Jiménez; Juan C Rubio; Pilar del Hoyo; F Bustos; Miguel A Martín; Ana Cabello; José R Ricoy; Joaquín Arenas
Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy.
Muscle & nerve 2002;25(2):185-8.
2001: Isabel Aguilera; José-Raúl García-Lozano; A Muñoz; Joaquín Arenas; Yolanda Campos; Isidoro Chinchón; A N Roldán; Juan Bautista
Mitochondrial DNA point mutation in the COI gene in a patient with McArdle's disease.
Journal of the neurological sciences 2001;192(1-2):81-4.
2001: Yolanda Campos; A García; J Eiris; M Fuster; Juan C Rubio; Miguel A Martín; Pilar del Hoyo; E Pintos; Manuel Castro-Gago; Joaquín Arenas
Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C > T mutation.
Journal of inherited metabolic disease 2001;24(6):685-7.
2001: Miguel A Martín; Juan C Rubio; J Buchbinder; R Fernández-Hojas; Pilar del Hoyo; Susana Teijeira; Josep Gámez; Carmen Navarro; J M Fernández; Ana Cabello; Yolanda Campos; Carlos Cervera; Jesus M Culebras; Antoni L Andreu; Robert J Fletterick; Joaquín Arenas
Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): a genotype-phenotype correlation study.
Annals of neurology 2001;50(5):574-81.
2001: EM Martínez Fernández; Alberto Gil-Peralta; R García-Lozano; Isidoro Chinchón; Isabel Aguilera; Olga Fernández-López; Joaquín Arenas; Yolanda Campos; Juan Bautista
Mitochondrial disease and stroke.
Stroke; a journal of cerebral circulation 2001;32(11):2507-10.
2001: Pilar de la Peña; Belén Bornstein; Pilar del Hoyo; Miguel Angel Fernández-Moreno; Miguel A Martín; Yolanda Campos; Carlos Gómez-Escalonilla; José Antonio Molina; Ana Cabello; Joaquín Arenas; Rafael Garesse
Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family.
Neurology 2001;57(7):1235-8.
2001: Yolanda Campos; Alberto García-Redondo; Miguel Angel Fernández-Moreno; M Martínez-Pardo; G Goda; Juan C Rubio; Miguel A Martín; Pilar del Hoyo; Ana Cabello; Belén Bornstein; Rafael Garesse; Joaquín Arenas
Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene.
Annals of neurology 2001;50(3):409-13.
2001: M de Toledo; Jaime Díaz-Guzmán; DA Pérez Martínez; RA Sáiz-Díaz; A Rodríguez-Vallejo; Yolanda Campos
[MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis].
Revista de neurologia 2001;33(2):148-50.
2001: Yolanda Campos; Josep Gámez; A García; Antoni L Andreu; Juan C Rubio; Miguel A Martín; Pilar del Hoyo; Carmen Navarro; Carlos Cervera; Rafael Garesse; Joaquín Arenas
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy.
Neuromuscular disorders : NMD 2001;11(5):477-80.
2001: Miguel A Martín; Juan C Rubio; A García; M A Fernández; Yolanda Campos; M Krawczak; D N Cooper; Joaquín Arenas
Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's disease.
Clinical genetics 2001;59(1):48-51.
2000: Miguel A Martín; Miguel Angel Gómez; F Guillén; B Börnstein; Yolanda Campos; Juan C Rubio; Carlos S de la Calzada; Joaquín Arenas
Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failure.
Biochimica et biophysica acta 2000;1502(3):330-6.
2000: Manuel Castro-Gago; Jesús Eirís; E Pintos; E Rodrigo; O Blanco-Barca; Yolanda Campos; Joaquín Arenas
[Benign congenital myopathy associated with a partial deficiency of complexes I and III of the mitochondrial respiratory chain]].
Revista de neurologia 2000;31(9):838-41.
2000: Yolanda Campos; gustavo lorenzo; Miguel A Martín; A Torregrosa; Pilar del Hoyo; Juan C Rubio; A García; Joaquín Arenas
A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes.
Neuromuscular disorders : NMD 2000;10(7):493-6.
2000: Juan C Rubio; Miguel A Martín; Pilar del Hoyo; Juan Bautista; Yolanda Campos; D Segura; Carmen Navarro; José R Ricoy; Ana Cabello; Joaquín Arenas
Molecular analysis of Spanish patients with AMP deaminase deficiency.
Muscle & nerve 2000;23(8):1175-8.
2000: Miguel A Martín; Juan C Rubio; Yolanda Campos; José R Ricoy; Ana Cabello; Joaquín Arenas
A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's disease.
Neuromuscular disorders : NMD 2000;10(6):447-9.
2000: Miguel Angel Fernández-Moreno; Belén Bornstein; Yolanda Campos; Joaquín Arenas; Rafael Garesse
The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genes.
Molecular genetics and metabolism 2000;70(3):238-40.
2000: Miguel A Martín; Juan C Rubio; Pilar del Hoyo; A García; F Bustos; Yolanda Campos; Ana Cabello; Jesus M Culebras; Joaquín Arenas
Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiency.
Human mutation 2000;15(6):579-80.
2000: A Muñoz-Málaga; Juan Bautista; J A Salazar; Isabel Aguilera; R Garcia; I Chinchon; M D Segura; Yolanda Campos; Joaquín Arenas
Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy?
Muscle & nerve 2000;23(4):538-42.
2000: Miguel A Martín; Juan C Rubio; Yolanda Campos; J Vílchez; Ana Cabello; Joaquín Arenas
Two homozygous mutations (R193W and 794/795 delAA) in the myophosphorylase gene in a patient with McArdle's disease.
Human mutation 2000;15(3):294.
2000: Juan C Rubio; Miguel A Martín; Yolanda Campos; Ana Cabello; Joaquín Arenas
A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle's disease.
Neuromuscular disorders : NMD 2000;10(2):138-40.
2000: Yolanda Campos; Miguel A Martín; C Caballero; Juan C Rubio; F de la Cruz; T Tuñón; Joaquín Arenas
Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstruction.
Neuromuscular disorders : NMD 2000;10(1):56-8.
1999: Miguel A Martín; Yolanda Campos; Maria Teresa García-Silva; Juan C Rubio; Pilar del Hoyo; Fernando de Bustos; A García; Joaquín Arenas
Slow segregation and rapid shift to homoplasmy coexist in a family with the T8993 > G mutation.
Journal of inherited metabolic disease 1999;22(8):939-40.
1999: Isabel Aguilera; José-Raúl García-Lozano; Juan Bautista; Yolanda Campos; Joaquín Arenas; Antonio Núñez-Roldán
A novel missense mutation 15747 T>C in the mitochondrial cytochrome b gene.
Human mutation 1999;14(6):545.
1999: E Franco; Juan Bautista; R Luque; Isidoro Chinchón; R García-Lozano; Isabel Aguilera; Yolanda Campos; Joaquín Arenas
[Mitochondrial encephalomyopathy of late presentation with progressive ophthalmoplegia, tremor and diffuse leukoencephalopathy].
Neurología (Barcelona, Spain) 1999;14(9):463-6.
1999: Miguel A Martín; Juan C Rubio; Fernando de Bustos; Pilar del Hoyo; Yolanda Campos; A García; B Börnstein; Ana Cabello; Joaquín Arenas
Molecular analysis in Spanish patients with muscle carnitine palmitoyltransferase deficiency.
Muscle & nerve 1999;22(7):941-3.
1999: Juan C Rubio; Miguel A Martín; A García; Yolanda Campos; Ana Cabello; Jesus M Culebras; Joaquín Arenas
McArdle's disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patient.
Neuromuscular disorders : NMD 1999;9(3):174-5.
1999: Joaquín Arenas; Yolanda Campos; Belén Bornstein; Renee Ribacoba; Miguel A Martín; Juan C Rubio; Filippo M Santorelli; M Zeviani; S DiMauro; Rafael Garesse
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers.
Neurology 1999;52(2):377-82.
1998: Juan C Rubio; Miguel A Martín; Juan Bautista; Yolanda Campos; D Segura; Ana Cabello; Isidoro Chinchón; Joaquín Arenas
Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chain.
Journal of the neurological sciences 1998;161(2):110-3.
1998: Joaquín Arenas; Juan C Rubio; Miguel A Martín; Yolanda Campos
Biological roles of L-carnitine in perinatal metabolism.
Early human development 1998;53 Suppl():S43-50.
1998: Yolanda Campos; Miguel A Martín; T García-Silva; Pilar del Hoyo; Juan C Rubio; Manuel Castro-Gago; J García-Peñas; J Casas; Ana Cabello; José R Ricoy; Joaquín Arenas
Clinical heterogeneity associated with mitochondrial DNA depletion in muscle.
Neuromuscular disorders : NMD 1998;8(8):568-73.
1998: Miguel A Martín; Yolanda Campos; Fernando de Bustos; Pilar del Hoyo; Juan C Rubio; Joaquín Arenas
[Molecular genetics of alterations in the mitochondrial respiratory chain].
Revista de neurologia 1998;26 Suppl 1():S27-35.
1998: Juan C Rubio; Miguel A Martín; Pilar del Hoyo; Fernando de Bustos; Yolanda Campos; Joaquín Arenas
[Enzyme complex defects of the mitochondrial respiratory chain].
Revista de neurologia 1998;26 Suppl 1():S15-20.
1998: J E Puñal; E Rodríguez; E Pintos; Yolanda Campos; Manuel Castro-Gago
Congenital ocular motor apraxia associated with myopathy, external hydrocephalus and NADH dehydrogenase deficiency.
Brain & development 1998;20(3):175-8.
1998: Joaquín Arenas; Yolanda Campos; Renee Ribacoba; Miguel A Martín; Juan C Rubio; P Ablanedo; Ana Cabello
Complex I defect in muscle from patients with Huntington's disease.
Annals of neurology 1998;43(3):397-400.
1998: B de los Reyes; J A Navarro; R Pérez-García; A Liras; Yolanda Campos; B Bornstein; Joaquín Arenas
Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia.
The American journal of clinical nutrition 1998;67(3):386-90.
1998: Belén Bornstein; R Huertas; Pilar Ochoa; Yolanda Campos; F Guillen; Rafael Garesse; Joaquín Arenas
Mitochondrial gene expression and respiratory enzyme activities in cardiac diseases.
Biochimica et biophysica acta 1998;1406(1):85-90.
1997: Yolanda Campos; Miguel A Martín; Juan C Rubio; M C Gutiérrez del Olmo; Ana Cabello; Joaquín Arenas
Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene.
Biochemical and biophysical research communications 1997;238(2):323-5.
1997: Maria Teresa García-Silva; Antonia Ribes; Yolanda Campos; Barbara Garavaglia; Joaquín Arenas
Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria.
Pediatric neurology 1997;17(2):165-70.
1997: Juan C Rubio; Miguel A Martín; Juan Bautista; Yolanda Campos; D Segura; Joaquín Arenas
Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'.
Neuromuscular disorders : NMD 1997;7(6-7):387-9.
1997: Yolanda Campos; Miguel A Martín; Juan C Rubio; L G Solana; C García-Benayas; J L Terradas; Joaquín Arenas
Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNA.
Neurology 1997;49(2):595-7.
1996: Joaquín Arenas; M R Gonzalez-Crespo; Yolanda Campos; M A Martin; Ana Cabello; Juan J Gomez Reino
Abnormal carnitine distribution in the muscles of patients with idiopathic inflammatory myopathy.
Arthritis and rheumatism 1996;39(11):1869-74.
1996: Yolanda Campos; Miguel A Martín; C Navarro; P Gordo; Joaquín Arenas
Single large-scale mitochondrial DNA deletion in a patient with mitochondrial myopathy associated with multiple symmetric lipomatosis.
Neurology 1996;47(4):1012-4.
1996: Miguel A Martín; José Antonio Molina; Félix Javier Jiménez-Jiménez; Julián Benito-León; M Ortí-Pareja; Yolanda Campos; Joaquín Arenas
Respiratory-chain enzyme activities in isolated mitochondria of lymphocytes from untreated Parkinson's disease patients. Grupo-Centro de Trastornos del Movimiento.
Neurology 1996;46(5):1343-6.
1996: Yolanda Campos; M A Martin; gustavo lorenzo; M Aparicio; Ana Cabello; Joaquín Arenas
Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.
Muscle & nerve 1996;19(2):187-90.
1996: Yolanda Campos; Miguel A Martín; Juan C Rubio; C Ricard; Ana Cabello; Joaquín Arenas
Multiple deletions of mitochondrial DNA in muscle from a patient with benign progressive external ophthalmoplegia.
Journal of inherited metabolic disease 1996;19(3):366-7.
1996: Yolanda Campos; Miguel A Martín; J Vaamonde; Ana Cabello; J Esteban; Joaquín Arenas
Clinical variability associated with the mutation at nucleotide position 8344 of the mitochondrial DNA.
Journal of inherited metabolic disease 1996;19(2):119-22.
1995: Joaquín Arenas; Yolanda Campos; Miguel A Martín
[Molecular genetics of mitochondrial cytopathologies].
Neurología (Barcelona, Spain) 1995;10 Suppl 1():44-9.
1995: Juan Bautista; A Muñoz-Málaga; Isidoro Chinchón; D Segura; J A Salazar; E Bescansa; Yolanda Campos; Joaquín Arenas
[Adult onset mitochondrial myopathy without ophthalmoplegia. Four cases attributable to complex III and IV deficits in the respiratory chain].
Neurología (Barcelona, Spain) 1995;10(8):319-23.
1995: Yolanda Campos; T Garcia-Silva; C R Barrionuevo; Ana Cabello; R Muley; Joaquín Arenas
Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.
Pediatric neurology 1995;13(1):69-72.
1995: Yolanda Campos; J Arenas; A Cabello; Juan J Gomez Reino
Respiratory chain enzyme defects in patients with idiopathic inflammatory myopathy.
Annals of the rheumatic diseases 1995;54(6):491-3.
1995: Yolanda Campos; Juan Bautista; E Gutiérrez-Rivas; D Chinchón; Ana Cabello; D Segura; Joaquín Arenas
Clinical heterogeneity in two pedigrees with the 3243 bp tRNA(Leu(UUR)) mutation of mitochondrial DNA.
Acta neurologica Scandinavica 1995;91(1):62-5.
1994: Maria Teresa García-Silva; Yolanda Campos; Antonia Ribes; Paz Briones; A Cabello; J Santos Borbujo; Joaquín Arenas; Barbara Garavaglia
Encephalopathy, petechiae, and acrocyanosis with ethylmalonic aciduria associated with muscle cytochrome c oxidase deficiency.
The Journal of pediatrics 1994;125(5 Pt 1):843-4.
1994: Javier Arpa; Yolanda Campos; Manuel Gutiérrez-Molina; Antonio Cruz-Martínez; Joaquín Arenas; Ana B Caminero; F Palomo; C Morales; P Barreiro
Benign mitochondrial myopathy with decreased succinate cytochrome C reductase activity.
Acta neurologica Scandinavica 1994;90(4):281-4.
1994: Javier Arpa; Yolanda Campos; Antonio Cruz-Martínez; Manuel Gutiérrez-Molina; Joaquín Arenas; M Alonso; I Plaza; C Morales; F Palomo; P Barreiro
[Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases].
Neurología (Barcelona, Spain) 1994;9(8):324-36.
1994: A Martínez-Bermejo; Ignacio Pascual-Castroviejo; Begoña Merinero; Yolanda Campos; V López-Martín; JM Arcas; Manuel Gutiérrez-Molina; Joaquín Arenas
[Complex I and IV deficits in the mitochondrial respiratory chain in two siblings with type I glutaric aciduria].
Neurología (Barcelona, Spain) 1994;9(7):303-6.
1994: Joaquín Arenas; R Huertas; Yolanda Campos; A E Díaz; J M Villalón; E Vilas
Effects of L-carnitine on the pyruvate dehydrogenase complex and carnitine palmitoyl transferase activities in muscle of endurance athletes.
FEBS letters 1994;341(1):91-3.
1994: Yolanda Campos; Juan Bautista; E Gutierrez-Rivas; J Llabrés; gustavo lorenzo; Joaquín Arenas
Variable clinical expression associated with the mutation 3243 np of mitochondrial DNA.
Journal of inherited metabolic disease 1994;17(5):634-5.
1993: Yolanda Campos; R Huertas; Juan Bautista; E Gutiérrez; M Aparicio; gustavo lorenzo; D Segura; M Villanueva; Ana Cabello; L Alesso
Muscle carnitine deficiency and lipid storage myopathy in patients with mitochondrial myopathy.
Muscle & nerve 1993;16(7):778-81.
1993: N Barroso; Yolanda Campos; R Huertas; J Esteban; J A Molina; A Alonso; E Gutierrez-Rivas; Joaquín Arenas
Respiratory chain enzyme activities in lymphocytes from untreated patients with Parkinson disease.
Clinical chemistry 1993;39(4):667-9.
1993: Yolanda Campos; R Huertas; gustavo lorenzo; Juan Bautista; E Gutiérrez; M Aparicio; L Alesso; Joaquín Arenas
Plasma carnitine insufficiency and effectiveness of L-carnitine therapy in patients with mitochondrial myopathy.
Muscle & nerve 1993;16(2):150-3.
1992: R Huertas; Yolanda Campos; E Díaz; J Esteban; L Vechietti; G Montanari; S D'Iddio; M Corsi; Joaquín Arenas
Respiratory chain enzymes in muscle of endurance athletes: effect of L-carnitine.
Biochemical and biophysical research communications 1992;188(1):102-7.
1992: Joaquín Arenas; R A Huertas; Yolanda Campos; Ana Cabello; E Gutierrez; Juan Bautista; D Segura
Oculopharyngeal muscular dystrophy and mitochondrial abnormalities.
Muscle & nerve 1992;15(9):1055-6.
1991: C Márquez; Juan Bautista; Joaquín Arenas; D Segura; Isidoro Chinchón; E Rafel; Yolanda Campos; R Huerta
[Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy].
Neurología (Barcelona, Spain) 1991;6(5):185-7.