Personas / Equipo Humano

Mªangels García Cazorla

Buscador de publicaciones

Publicaciones

  • Posset R, Garbade SF, Boy N, Burlina AB, Dionisi-Vici C, Dobbelaere D, Garcia-Cazorla A, de Lonlay P, Teles EL, Vara R, Mew NA, Batshaw ML, Baumgartner MR, McCandless S, Seminara J, Summar M, Hoffmann GF, Kölker S, Burgard P and Additional individual contributors of the UCDC and the E-IMD consortium.

    Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders-A successful strategy for clinical research of rare diseases.

    JOURNAL OF INHERITED METABOLIC DISEASE . 42(1): 93-106. Nº de citas: 43

    [doi:10.1002/jimd.12031]

  • Saudubray JM and Garcia-Cazorla A.

    An overview of inborn errors of metabolism affecting the brain: from neurodevelopment to neurodegenerative disorders

    Dialogues in Clinical Neuroscience . 20(4): 301-325. Nº de citas: 83

    [doi:10.31887/DCNS.2018.20.4/jmsaudubray]

  • Cortés-Saladelafont E, Lipstein N and Garcia-Cazorla A.

    Presynaptic disorders: a clinical and pathophysiological approach focused on the synaptic vesicle

    JOURNAL OF INHERITED METABOLIC DISEASE . 41(6): 1131-1145. Nº de citas: 7

    [doi:10.1007/s10545-018-0230-z]

  • Garcia-Cazorla A and Saudubray JM.

    Cellular neurometabolism: a tentative to connect cell biology and metabolism in neurology

    JOURNAL OF INHERITED METABOLIC DISEASE . 41(6): 1043-1054. Nº de citas: 20

    [doi:10.1007/s10545-018-0226-8]

  • Tristan-Noguero A and Garcia-Cazorla A.

    Synaptic metabolism: a new approach to inborn errors of neurotransmissionKeywords

    JOURNAL OF INHERITED METABOLIC DISEASE . 41(6): 1065-1075. Nº de citas: 11

    [doi:10.1007/s10545-018-0235-7]

  • Batllori-Tragant M, Molero M, Ormazabal-Herrero A, Montero-Sanchez R, Sierra-March C, Ribes A, Montoya C, Ruiz-Pesini E, O'Callaghan-Gordo M, Pias L, Nascimento-Osorio A, Palau F, Armstrong-Moron J, Yubero-Siles D, Ortigoza-Escobar JD, Garcia-Cazorla A and Artuch-Iriberri R.

    Cerebrospinal fluid monoamines, pterins, and folate in patients with mitochondrial diseases: systematic review and hospital experience

    JOURNAL OF INHERITED METABOLIC DISEASE . 41(6): 1147-1158. Nº de citas: 13

    [doi:10.1007/s10545-018-0224-x]

  • Tonduti D, Panteghini C, Pichiecchio A, Decio A, Carecchio M, Reale C, Moroni I, Nardocci N, Campistol-Plana J, Garcia-Cazorla A, Pérez-Dueñas B, Cerebral Calcification International Study Group, Chiapparini L, Garavaglia B and Orcesi S.

    Encephalopathies with intracranial calcification in children: clinical and genetic characterization

    Orphanet Journal of Rare Diseases . 13: 135-135. Nº de citas: 23

    [doi:10.1186/s13023-018-0854-y]

  • Cortés-Saladelafont E, Molero M, Cuadras-Palleja D, Casado-Rio M, Armstrong-Moron J, Yubero-Siles D, Montoya J, Artuch-Iriberri R and Garcia-Cazorla A.

    Gamma-aminobutyric acid levels in cerebrospinal fluid in neuropaediatric disorders

    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 60(8): 780-792. Nº de citas: 9

    [doi:10.1111/dmcn.13746]

  • Chakrapani A, Valayannopoulos V, Segarra NG, Del Toro M, Donati MA, Garcia-Cazorla A, González MJ, Plisson C and Giordano V.

    Effect of carglumic acid with or without ammonia scavengers on hyperammonaemia in acute decompensation episodes of organic acidurias

    Orphanet Journal of Rare Diseases . 13: 97-97. Nº de citas: 16

    [doi:10.1186/s13023-018-0840-4]

  • Saudubray JM and Garcia-Cazorla A.

    Inborn Errors of Metabolism Overview Pathophysiology, Manifestations, Evaluation, and Management

    PEDIATRIC CLINICS OF NORTH AMERICA . 65(2): 179-208. Nº de citas: 173

    [doi:10.1016/j.pcl.2017.11.002]