Výsledky vyhledávání

Neonatal Diagnosis, Treatment and Related Factors of Congenital Dislocation of the Hip

Autor: Levine Db, Lim Wn, Philip D. Wilson, Artz Td, Eduardo A. Salvati

Publikováno v: Clinical Orthopaedics and Related Research. 110:112-136

The unstable hip can be diagnosed in newborns with acceptable accuracy. The following factors are associated with the newborn unstable hip: female preponderance, breech presentations, cesarean section deliveries, first borns, left hip involvement, th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e4c61a66d35e917f0572a1ca46525d9
https://doi.org/10.1097/00003086-197507000-00015

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A NEW ACID MUCOPOLYSACCHARIDOSIS WITH SKELETAL DEFORMITIES SIMULATING RHEUMATOID ARTHRITIS

Autor: Winchester P, Danes Bs, Grossman H, Lim Wn

Publikováno v: American Journal of Roentgenology. 106:121-128

Two siblings are described with biochemical evidence of mucopolysaccharide storage presumably inherited as an autosomal recessive.[See figure in the PDF file]The syndrome is characterized by a progressive grotesque deformity due to intra-articular de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dc90230a5ce52faeed41bde4a63ff42
https://doi.org/10.2214/ajr.106.1.121

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Akademický článek

Oral supplementation of L-glutathione prevents ultraviolet B-induced melanogenesis and oxidative stress in BALB/c mice.

Autor: Nagapan TS; Programme of Biomedical Science, Centre of Health & Applied Sciences, Faculty of Health Sciences, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia., Lim WN; Programme of Biomedical Science, Centre of Health & Applied Sciences, Faculty of Health Sciences, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia., Basri DF; Programme of Biomedical Science, Centre of Health & Applied Sciences, Faculty of Health Sciences, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia., Ghazali AR; Programme of Biomedical Science, Centre of Health & Applied Sciences, Faculty of Health Sciences, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia.

Publikováno v: Experimental animals [Exp Anim] 2019 Nov 06; Vol. 68 (4), pp. 541-548. Date of Electronic Publication: 2019 Jun 26.

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Akademický článek

Complexity of the Genetics and Clinical Presentation of Spinocerebellar Ataxia 17.

Autor: Nethisinghe S; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, United Kingdom., Lim WN; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, United Kingdom., Ging H; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, United Kingdom., Zeitlberger A; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, United Kingdom., Abeti R; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, United Kingdom., Pemble S; Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom., Sweeney MG; Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom., Labrum R; Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom., Cervera C; Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom., Houlden H; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, United Kingdom.; MRC Centre for Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, United Kingdom., Rosser E; Department of Clinical Genetics, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom., Limousin P; Sobell Department of Motor Neuroscience and Movement Disorders, UCL Queen Square Institute of Neurology, London, United Kingdom., Kennedy A; Chelsea and Westminster Hospital, London, United Kingdom., Lunn MP; Department of Neuroimmunology, UCL Queen Square Institute of Neurology, London, United Kingdom., Bhatia KP; Sobell Department of Motor Neuroscience and Movement Disorders, UCL Queen Square Institute of Neurology, London, United Kingdom., Wood NW; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, United Kingdom., Hardy J; Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, United Kingdom.; The Reta Lila Weston Institute of Neurological Studies, UCL Queen Square Institute of Neurology, London, United Kingdom., Polke JM; Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom., Veneziano L; Istituto di Farmacologia Traslazionale - National Research Council, Rome, Italy., Brusco A; Department of Medical Sciences, University of Turin, Turin, Italy.; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, Turin, Italy., Davis MB; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, United Kingdom., Giunti P; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, United Kingdom.

Publikováno v: Frontiers in cellular neuroscience [Front Cell Neurosci] 2018 Nov 23; Vol. 12, pp. 429. Date of Electronic Publication: 2018 Nov 23 (Print Publication: 2018).

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