182 results on '"Pellissier, Jean-François"'
Search Results
152. Exclusion of muscle specific actinin-associated LIM protein (ALP) gene from 4q35 facioscapulohumeral muscular dystrophy (FSHD) candidate genes
153. Stüve-Wiedemann syndrome and defects of the mitochondrial respiratory chain
154. Expression of cell adhesion molecules in normal nerves, chronic axonal neuropathies and Schwann cell tumors
155. Lafora disease is not linked to the Unverricht-Lundborg locus
156. Quantitative imaging of estrogen and progesterone receptors, estrogen-regulated protein, and growth fraction: immunocytochemical assays in 52 meningiomas
157. Polymyalgia rheumatica and mitochondrial myopathy: Clinicopathologic and biochemical studies in five cases
158. Myopathy with hexagonally cross-linked crystalloid inclusions: Delineation of a clinico-pathological entity
159. The lipid phosphatase myotubularin is essential for skeletal muscle maintenance but not for myogenesis in mice.
160. Rapid diagnosis of human prion disease using streptomycin with tonsil and brain tissues.
161. Platelet-Endothelial Cell Adhesion Molecule-1 and CD146: Soluble Levels and in Situ Expression of Cellular Adhesion Molecules Implicated in the Cohesion of Endothelial Cells in Idiopathic Inflammatory Myopathies
162. Lethal injection of potassium chloride: first description of the pathological appearance of organs.
163. HLADRB1*01 and macrophagic myofasciitis
164. Semi-Late Onset and Rapidly Progressive Case of Lafora’s Disease with Predominant Cognitive Symptoms
165. Further heterogeneity in myopathy with tubular aggregates?
166. MRI and 31PMR Spectroscopy Investigations of Muscle Function Disclose No Abnormality in Macrophagic Myofasciitis
167. Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay.
168. Nuclear Inherited Mitochondriopathy with mtDNA Multiple Deletions.
169. Metastatic Cerebral Abscesses due to Hemophilus paraphrophilus
170. Rapidly Progressive Dementia and Myoclonus.
171. Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): A clinical, biochemical and molecular study
172. CNS Axonal Regeneration within Peripheral Nerve Grafts Cryopreserved by Vitrification: Cytological and Functional Aspects
173. Combination of histopathological and electromyographic patterns can help to evaluate functional outcome of critical ill patients with neuromuscular weakness syndromes
174. Nemaline myopathy caused by mutations in the nebulin gene may present as a distal myopathy
175. [Potassium channelopathies and Morvan's syndromes].
176. Rapid diagnosis of human prion disease using streptomycin with tonsil and brain tissues.
177. [Limbic encephalitis--evolving concepts].
178. Focal myositis associated with S-1 radiculopathy: report of two cases.
179. Cytokines, chemokines, and cell adhesion molecules in inflammatory myopathies.
180. [BK virus-induced tubulo-interstitial nephritis in a renal transplant recipient].
181. [Renal pathology: a rare association of immunoglobulin deposits].
182. [Dysferlinopathy. Example of a new myopathy].
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