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Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|May 25, 2015
Relationship between GII.3 norovirus infections and blood group antigens in young children in TunisiaS Ayouni, M Estienney, K Sdiri-Loulizi, et al.European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|December 4, 2010
Epidemiology and clinical features of gastroenteritis in hospitalised children: prospective survey during a 2-year period in a Parisian hospital, FranceM Lorrot, F Bon, M J El Hajje, et al.The Journal of Investigative Dermatology|April 1, 1997
Premature termination codons are present on both alleles of the bullous pemphigoid antigen 2/type XVII collagen gene in five Austrian families with generalized atrophic benign epidermolysis bullosaT N Darling, J A McGrath, C Yee, et al.The British Journal of Dermatology|January 20, 1999
Pyloric atresia-junctional epidermolysis bullosa syndrome: mutations in the integrin beta4 gene (ITGB4) in two unrelated patients with mild diseaseJ E Mellerio, L Pulkkinen, J R McMillan, et al.The Journal of Hospital Infection|December 6, 2014
Is surgical site scrubbing before painting of value? Review and meta-analysis of clinical studiesA Lefebvre, P Saliou, O Mimoz, et al.Diagnostic and Interventional Imaging|May 1, 2019
Endovascular stenting for chronic femoro-iliac venous obstructive disease: Clinical efficacy and short-term outcomesK Guillen, N Falvo, M Nakai, et al.The American Journal of Pathology|February 13, 2001
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiencyJ W Bauer, F Rouan, B Kofler, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|December 4, 2021
Ichthyosis, psoriasiform dermatitis, and recurrent fungal infections in patients with biallelic mutations in PERPL Youssefian, S Khodavaisy, F Khosravi-Bachehmir, et al.The Journal of Investigative Dermatology|November 1, 1992
Genetic linkage between the collagen VII (COL7A1) gene and the autosomal dominant form of dystrophic epidermolysis bullosa in two Dutch kindredsN A Gruis, J N Bavinck, P M Steijlen, et al.Muscle & Nerve|September 13, 2006
Plectin defects in epidermolysis bullosa simplex with muscular dystrophyJ R McMillan, M Akiyama, F Rouan, et al.Pageof 67