Resultados globales: 4 registros encontrados en 0.02 segundos.
Artículos, Encontrados 2 registros
Materiales académicos, Encontrados 2 registros
Artículos Encontrados 2 registros  
1.
16 p, 3.8 MB Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia / Tuschl, Karin (University College London. Institute of Child Health) ; Meyer, Esther (University College London. Institute of Child Health) ; Valdivia, Leonardo E. (University College London. Department of Cell and Developmental Biology) ; Zhao, Ningning (Oregon Health and Science University. Department of Cell, Development and Cancer Biology) ; Dadswell, Chris (University of Sussex. Department of Chemistry, School of Life Sciences) ; Abdul-Sada, Alaa (University of Sussex. Department of Chemistry, School of Life Sciences) ; Hung, Christina Y. (Harvard Medical School. Division of Genetics and Genomics) ; Simpson, Michael A. (King's College London School of Medicine. Division of Genetics and Molecular Medicine) ; Chong, W.K. (Great Ormond Street Hospital for Children. Department of Radiology (Londres)) ; Jacques, Thomas S. (Great Ormond Street Hospital for Children. Department of Histopathology (Londres)) ; Woltjer, Randy L. (Oregon Health and Science University. Department of Pathology) ; Eaton, Simon (University College London. Institute of Child Health) ; Gregory, Allison (Oregon Health and Science University. Department of Molecular and Medical Genetics) ; Sanford, Lynn (Oregon Health and Science University. Department of Molecular and Medical Genetics) ; Kara, Eleanna (University College London. Institute of Neurology) ; Houlden, Henry (University College London. Institute of Neurology) ; Cuno, Stephan M. (Technical University of Munich. Institute of Human Genetics) ; Prokisch, Holger (Technical University of Munich. Institute of Human Genetics) ; Valletta, Lorella (Oregon Health and Science University. Department of Molecular and Medical Genetics) ; Tiranti, Valeria (Oregon Health and Science University. Department of Molecular and Medical Genetics) ; Younis, Rasha (University of Birmingham. Department of Medical and Molecular Genetics) ; Maher, Eamonn R. (University of Birmingham. Centre for Rare Diseases and Personalised Medicine) ; Spencer, John (University of Sussex. Department of Chemistry, School of Life Sciences) ; Straatman Iwanowska, Ania (University College London. Laboratory for Molecular Cell Biology and Cell Biology Unit) ; Gissen, Paul (University College London. Institute of Child Health) ; Selim, Laila A.M. (Cairo University Children's Hospital. Department of Paediatric Neurology) ; Pintos Morell, Guillem (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Coroleu Lletget, Wifredo (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Mohammad, Shekeeb S. (University of Sydney. Institute for Neuroscience and Muscle Research) ; Yoganathan, Sangeetha (Christian Medical College Hospital. Department of Neurological Sciences (Vellore, Índia)) ; Dale, Russell C. (University of Sydney. Institute for Neuroscience and Muscle Research) ; Thomas, Maya (Christian Medical College Hospital. Department of Neurological Sciences (Vellore, Índia)) ; Rihel, Jason (University College London. Department of Cell and Developmental Biology) ; Bodamer, Olaf A. (Harvard Medical School. Division of Genetics and Genomics) ; Enns, Caroline A. (Oregon Health & Sciences University. Department of Cell, Development and Cancer Biology) ; Hayflick, Susan J. (Oregon Health and Science University. Department of Molecular and Medical Genetics) ; Clayton, Peter T. (University College London. Institute of Child Health) ; Mills, Philippa B. (University College London. Institute of Child Health) ; Kurian, Manju A. (University College London. Institute of Child Health) ; Wilson, Stephen W. (University College London. Department of Cell and Developmental Biology)
Although manganese is an essential trace metal, little is known about its transport and homeostatic regulation. Here we have identified a cohort of patients with a novel autosomal recessive manganese transporter defect caused by mutations in SLC39A14. [...]
2016 - 10.1038/ncomms11601
Nature communications, Vol. 7 Núm. 11601 (May 2016)  
2.
12 p, 7.8 MB Alcohol Consumption during Pregnancy : Analysis of Two Direct Metabolites of Ethanol in Meconium / Sanvisens, Arantza (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Robert, Neus (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Hernández Pérez, José María (Institut Germans Trias i Pujol) ; Zuluaga, Paola (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Farré Albaladejo, Magí (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Coroleu, Wifredo (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Serra Landete, Montserrat (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Tor Aguilera, J. (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Muga Bustamante, Robert (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Universitat Autònoma de Barcelona
Alcohol consumption in young women is a widespread habit that may continue during pregnancy and induce alterations in the fetus. We aimed to characterize prevalence of alcohol consumption in parturient women and to assess fetal ethanol exposure in their newborns by analyzing two direct metabolites of ethanol in meconium. [...]
2016 - 10.3390/ijms17030417
International Journal of Molecular Sciences, Vol. 17 Núm. 3 (March 2016)  

Materiales académicos Encontrados 2 registros  
1.
5 p, 81.9 KB Perinatologia [103651] / Rodrigo Gonzalo de Liria, Carlos ; Coroleu Lletget, Wifredo ; Guinovart Galiana, Gemma ; Badia Barnussell, Joan ; Castillo Salinas, Félix ; Universitat Autònoma de Barcelona. Facultat de Medicina
Es tracta d'una assignatura optativa que es pot cursar a partir del quart curs i que té com a objectiu general que l'estudiant es familiaritzi amb la pràctica professional en context real de la Perinatologia.
Se trata de una asignatura optativa que se puede cursar a partir del cuarto curso y que tiene como objetivo general que el estudiante se familiarice con la práctica profesional en contexto real de la perinatología.

2018-19
Grau en Medicina [1192]
2 documentos
2.
5 p, 82.3 KB Perinatologia [103651] / Rodrigo Gonzalo de Liria, Carlos ; Coroleu Lletget, Wifredo ; Pérez Picañol, Emilio ; Guinovart Galiana, Gemma ; Badia Barnussell, Joan ; Castillo Salinas, Félix ; Universitat Autònoma de Barcelona. Facultat de Medicina
Es tracta d'una assignatura optativa que es pot cursar a partir del quart curs i que té com a objectiu general que l'estudiant es familiaritzi amb la pràctica professional en context real de la Perinatologia.
Se trata de una asignatura optativa que se puede cursar a partir del cuarto curso y que tiene como objetivo general que el estudiante se familiarice con la práctica profesional en contexto real de la perinatología.

2017-18
Grau en Medicina [1192]
2 documentos

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