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Diffuse hair loss in Addison disease: a reason for X-linked adrenoleukodystrophy screening.
Lecumberri B, Girós ML, Coll MJ, Marco A, Casado M, Pallardo LF, Pardo J. Lecumberri B, et al. Among authors: giros ml. J Am Acad Dermatol. 2012 May;66(5):860-1. doi: 10.1016/j.jaad.2011.09.003. J Am Acad Dermatol. 2012. PMID: 22507581 No abstract available.
[X- linked adrenoleukodystrophy: misdiagnosed disease in children with idiopathic Addison's disease].
García Cuartero B, González Vergaz A, Herranz Antolín S, Blanco C, Sánchez Mateos M, Carrasco Marina L, Gutiérrez Solana L, Girós M. García Cuartero B, et al. An Pediatr (Barc). 2008 Apr;68(4):404-5. doi: 10.1157/13117717. An Pediatr (Barc). 2008. PMID: 18394390 Spanish. No abstract available.
Clinical and molecular diagnosis of non-phosphomannomutase 2 N-linked congenital disorders of glycosylation in Spain.
Medrano C, Vega A, Navarrete R, Ecay MJ, Calvo R, Pascual SI, Ruiz-Pons M, Toledo L, García-Jiménez I, Arroyo I, Campo A, Couce ML, Domingo-Jiménez MR, García-Silva MT, González-Gutiérrez-Solana L, Hierro L, Martín-Hernández E, Martínez-Pardo M, Roldán S, Tomás M, Cabrera JC, Mártinez-Bugallo F, Martín-Viota L, Vitoria-Miñana I, Lefeber DJ, Girós ML, Serrano Gimare M, Ugarte M, Pérez B, Pérez-Cerdá C. Medrano C, et al. Among authors: giros ml. Clin Genet. 2019 May;95(5):615-626. doi: 10.1111/cge.13508. Epub 2019 Apr 3. Clin Genet. 2019. PMID: 30653653
Sitosterolemia: Diagnosis, Metabolic and Hematological Abnormalities, Cardiovascular Disease and Management.
Bastida JM, Girós ML, Benito R, Janusz K, Hernández-Rivas JM, González-Porras JR. Bastida JM, et al. Among authors: giros ml. Curr Med Chem. 2019;26(37):6766-6775. doi: 10.2174/0929867325666180705145900. Curr Med Chem. 2019. PMID: 29984642 Review.
A Population-Based Study on Congenital Disorders of Protein N- and Combined with O-Glycosylation Experience in Clinical and Genetic Diagnosis.
Pérez-Cerdá C, Girós ML, Serrano M, Ecay MJ, Gort L, Pérez Dueñas B, Medrano C, García-Alix A, Artuch R, Briones P, Pérez B. Pérez-Cerdá C, et al. Among authors: giros ml. J Pediatr. 2017 Apr;183:170-177.e1. doi: 10.1016/j.jpeds.2016.12.060. Epub 2017 Jan 27. J Pediatr. 2017. PMID: 28139241
Evaluation of the preventive effect of glyceryl trioleate-trierucate ("Lorenzo's oil") therapy in X-linked adrenoleukodystrophy: results of two concurrent trials.
Moser HW, Raymond GV, Koehler W, Sokolowski P, Hanefeld F, Korenke GC, Green A, Loes DJ, Hunneman DH, Jones RO, Lu SE, Uziel G, Giros ML, Roels F. Moser HW, et al. Among authors: giros ml. Adv Exp Med Biol. 2003;544:369-87. doi: 10.1007/978-1-4419-9072-3_47. Adv Exp Med Biol. 2003. PMID: 14713253 Clinical Trial. No abstract available.
Galactosaemia presenting as congenital pseudoafibrinogenaemia.
Ruiz M, Jover S, Armas M, Duque MR, Santana C, Girós ML, Boleda MD. Ruiz M, et al. Among authors: giros ml. J Inherit Metab Dis. 1999 Dec;22(8):943-4. doi: 10.1023/a:1005660011709. J Inherit Metab Dis. 1999. PMID: 10604151 No abstract available.
Neuronopathic juvenile glucosylceramidosis due to sap-C deficiency: clinical course, neuropathology and brain lipid composition in this Gaucher disease variant.
Pàmpols T, Pineda M, Girós ML, Ferrer I, Cusi V, Chabás A, Sanmarti FX, Vanier MT, Christomanou H. Pàmpols T, et al. Among authors: giros ml. Acta Neuropathol. 1999 Jan;97(1):91-7. doi: 10.1007/s004010050960. Acta Neuropathol. 1999. PMID: 9930900
[Smith-Lemli-Opitz syndrome: abnormal cholesterol biosynthesis].
de la Torre Verdú M, Vázquez López M, Carrasco Marina L, Girós ML, Quijano Roy S, Arregui Sierra A. de la Torre Verdú M, et al. Among authors: giros ml. An Esp Pediatr. 1997 Jun;46(6):617-20. An Esp Pediatr. 1997. PMID: 9297435 Spanish. No abstract available.
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