C. Gómez‐Lado

发表

[Pontocerebellar hypoplasia type I and mitochondrial pathology].

M. Castro‐Gago, J. Eirís-Puñal, C. Gómez‐Lado, 2007, Revista de neurologia.

Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration: a late onset variant of PCH-1?

M. Castro‐Gago, J. Eirís-Puñal, C. Gómez‐Lado, 2009, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Primary Adenosine Monophosphate (AMP) Deaminase Deficiency in a Hypotonic Infant

M. Castro‐Gago, Miguel Ángel Martín, I. García‐Consuegra, 2011, Journal of child neurology.

Hashimoto encephalopathy in a preschool girl.

M. Castro‐Gago, J. Eirís-Puñal, C. Gómez‐Lado, 2010, Pediatric neurology.

Evolution of subclinical hypothyroidism in children treated with antiepileptic drugs.

M. Castro‐Gago, S. Rodriguez-Segade, J. Eirís-Puñal, 2007, Pediatric neurology.

Letter to the Editor

M. Castro‐Gago, J. Eirís-Puñal, C. Gómez‐Lado, 2006 .

The Influence of Valproic Acid and Carbamazepine Treatment on Serum Biotin and Zinc Levels and on Biotinidase Activity

M. Castro‐Gago, S. Rodriguez-Segade, L. Pérez-Gay, 2011, Journal of child neurology.

Serum Biotinidase Activity in Children Treated With Valproic Acid and Carbamazepine

M. Castro‐Gago, J. Eirís-Puñal, C. Gómez‐Lado, 2010, Journal of child neurology.

Clinical and neurophysiological response to ephedrine in a patient affected with slow-channel congenital myasthenic syndrome.

J. Pardo, J. Eirís-Puñal, L. Pérez-Gay, 2020, Revista de neurologia.

Copy number variation analysis of patients with intellectual disability from North-West Spain.

Á. Carracedo, R. Cruz, M. Castro‐Gago, 2017, Gene.

Clinical description, molecular delineation, and genotype-phenotype correlation in KBG syndrome: 67 new patients and review of the literature.

Lago, I. Mahillo, B. Gener, 2022, medRxiv.

Growth in children and adolescents with mitochondrial diseases

M. Castro‐Gago, J. Eirís-Puñal, L. Pérez-Gay, 2011, Journal of Pediatric Neurology.

Interstitial microdeletions including the chromosome band 4q13.2 and the UBA6 gene as possible causes of intellectual disability and behavior disorder

Á. Carracedo, M. Castro‐Gago, I. Quintela, 2015, American journal of medical genetics. Part A.

Juvenile xanthogranuloma of the cauda equina.

M. Castro‐Gago, A. Alonso, B. Vieites, 2009, Pediatric neurology.

Congenital Hypothyroidism with Neurological and Respiratory Alterations: A Case Detected Using a Variable Diagnostic Threshold for TSH

Luis Antonio Castaño, M. Couce, J. Barreiro, 2011, Journal of clinical research in pediatric endocrinology.

Treatment of mitochondrial encephalomyopathies with a xanthine oxidase inhibitor.

M. Castro‐Gago, S. Rodriguez-Segade, J. Eirís-Puñal, 2006, Pediatric neurology.

Respiratory chain complex I deficiency in an infant with Ohtahara syndrome

M. Castro‐Gago, J. Eirís-Puñal, C. Gómez‐Lado, 2009, Brain and Development.

Cardiac troponin I for accurate evaluation of cardiac status in myopathic patients

M. Castro‐Gago, J. Eirís-Puñal, C. Gómez‐Lado, 2009, Brain and Development.

Duane's syndrome and 22 marker chromosome: A possible cat‐eye syndrome

M. Castro‐Gago, J. Eirís, C. Gómez‐Lado, 2006, Acta paediatrica.

Abnormal myelination in Angelman syndrome.

M. Castro‐Gago, Manuel Castro-Gago, Carmen Gómez-Lado, 2010, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Intrathecal baclofen for progressive neurological disease in children.

M. Castro‐Gago, L. Pérez-Gay, C. Gómez‐Lado, 2013, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Clinical description, molecular delineation and genotype–phenotype correlation in 340 patients with KBG syndrome: addition of 67 new patients

Lago, I. Mahillo, B. Gener, 2022, Journal of Medical Genetics.

Levels of leptin, insulin, IGF-I, IGFBP-3, IL-6 and IL-8 in sera of patients with muscular dystrophy and mitochondrial encephalomyopathy

M. Castro‐Gago, S. Rodriguez-Segade, J. Rodriguez-Garcia, 2010, Journal of Pediatric Neurology.

[Reversible posterior leukoencephalopathy syndrome: an infrequent complication in the course of haemolytic-uremic syndrome].

M. Castro‐Gago, F. Martinón-Torres, A. Rodríguez-Núñez, 2007, Revista de neurologia.