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Orthodontic dental movement and its association with the presence of gingival recession
(Facultad de Odontología, 2017)
Overdenture as a restorative option for hypocalcified-hypoplastic amelogenesis imperfecta: a case report.
(2009-08-06)
AIM: The aim of this report is to describe the restorative treatment of an 18-year-old patient diagnosed with autosomal recessive hypocalcified-hypoplastic amelogenesis imperfecta (AI). BACKGROUND: Esthetic and functional ...
Non-inflammatory destructive periodontal disease
(2016-03-01)
Background: Non-Inflammatory Destructive Periodontal Disease (NIDPD), is a severe destructive periodontal disease, that is characterized by the attachment loss and alveolar bone loss, without signs of the gingival inflammation, ...
Dusty core disease' (DuCD): expanding morphological spectrum of RYR1 recessive myopathies
(2019)
Several morphological phenotypes have been associated to RYR1-recessive myopathies. We recharacterized the RYR1-recessive morphological spectrum by a large monocentric study performed on 54 muscle biopsies from a large ...
'Dusty core disease' (DuCD): expanding morphological spectrum of RYR1 recessive myopathies
(NLM (Medline), 2019)
Several morphological phenotypes have been associated to RYR1-recessive myopathies. We recharacterized the RYR1-recessive morphological spectrum by a large monocentric study performed on 54 muscle biopsies from a large ...
Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3
(Neurimuscular Disorder 14 (5) 301-306, 2004)
Cbarcot-Marie-Tooth disease (CMT) comprises a heterogeneous group of hereditary motor and sensory peripheral neuropathies. The
autosomal recessive axonal form of CMT (ARCMT2) is ram. Eight patients of a large consanguineous ...
Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3
(Neurimuscular Disorder 14 (5) 301-306, 2004)
Cbarcot-Marie-Tooth disease (CMT) comprises a heterogeneous group of hereditary motor and sensory peripheral neuropathies. The
autosomal recessive axonal form of CMT (ARCMT2) is ram. Eight patients of a large consanguineous ...
HLA COMPLEX IN WERNER'S DISEASE
(Clinical Immunology National Center and National Center for Rheumatic Diseases, SAS-UCV., 2016)
Treatment of gingival recession with collagen membrane and DFDBA: A histometric study in dogs
(2009-12-28)
In a previous study, we evaluated the findings related to the use of resorbable collagen membranes in humans along with DFDBA (demineralized freeze-dried bone allograft). The aim of this subsequent study was to histometrically ...
Treatment of gingival recession with collagen membrane and DFDBA: A histometric study in dogs
(2009-12-28)
In a previous study, we evaluated the findings related to the use of resorbable collagen membranes in humans along with DFDBA (demineralized freeze-dried bone allograft). The aim of this subsequent study was to histometrically ...