15 documents found, page 1 of 2

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DNM2 mutations in a cohort of sporadic patients with centronuclear myopathy

Abath Neto,Osorio; Martins,Cristiane de Araújo; Carvalho,Mary; Chadi,Gerson; Seitz,Katia Werneck; Oliveira,Acary Souza Bulle; Reed,Umbertina Conti

Centronuclear myopathy (CNM) is a rare congenital muscle disease characterized by fibers with prominent centralized nuclei in muscle biopsies. The disease is clinically heterogeneous, ranging from severe neonatal hypotonic phenotypes to adult-onset mild muscle weakness, and can have multiple modes of inheritance in association with various genes, including MTM1, DNM2, BIN1 and RYR1. Here we analyzed 18 sporadic...

Date: 2015   |   Origin: Oasisbr

Does dexamethasone act in neuropeptides SP and CGRP in neurogenic inflammation ...

Freitas,Jose Octavio Gonçalves de; Quieregatto,Paulo Rogério; Hochman,Bernardo; Lapin,Guilherme Abbud Franco; Mella,Stella Maria Botequio

PURPOSE: To investigate the neuropeptides substance P (SP) and calcitonin gene-related peptide (CGRP) after subcutaneous injection of dexamethasone prior to skin incision in rats.METHODS:Twenty seven Wistar-EPM-1 rats were randomly divided into three groups. The sham group (SG) of rats was injected with 0.9 % saline. The second group (Dexa) was injected with 1.0 mg/kg dexamethasone, and the third group (Dexa+) ...

Date: 2015   |   Origin: Oasisbr

Clinical aspects of patients with sarcoglycanopathies under steroids therapy

Albuquerque,Marco A. V.; Abath-Neto,Osório; Maximino,Jéssica R.; Chadi,Gerson; Zanoteli,Edmar; Reed,Umbertina C.

Patients with sarcoglycanopathies, which comprise four subtypes of autosomal recessive limb-girdle muscular dystrophies, usually present with progressive weakness leading to early loss of ambulation and premature death, and no effective treatment is currently available. Objective To present clinical aspects and outcomes of six children with sarcoglycanopathies treated with steroids for at least one year. Method...

Date: 2014   |   Origin: Oasisbr

Effects of subcutaneous carbon dioxide on calcitonin gene related peptide and s...

Raymundo,Erica Calcagno; Hochman,Bernardo; Nishioka,Michele Akemi; Freitas,José Octávio Gonçalves de; Maximino,Jéssica Ruivo; Chadi,Gerson

PURPOSE: To investigate the subcutaneous injection of carbon dioxide (CO2) on neuropeptides Calcitonin Gene-Related Peptide (CGRP) and Substance P (SP) secretion in rat skin.METHODS: Fifty-six Wistar-EPM rats were distributed in two groups: one for CGRP analysis, the other for SP analysis. Each group was subdivided into four subgroups: control (Cont), control with needle (ContNd), CO2 injection (CO2Inj) and atm...

Date: 2014   |   Origin: Oasisbr

Duchenne muscular dystrophy and Duane's syndrome: a rare association

Pasqualin,Lívia M.A.; Zanoteli,Edmar; Veloso,Marco A.M.; Frizzo,Silvana K.; Resende,Maria B.D.; Abucham-Neto,Julio Z.; Polati,Mariza; Chadi,Gerson

Date: 2013   |   Origin: Oasisbr

Spinal cord injury as a trigger to develop periodic leg movements during sleep:...

Telles,Susana Cristina Lerosa; Alves,Rosana S. Cardoso; Chadi,Gerson

The primary trigger to periodic limb movement (PLM) during sleep is still unknown. Its association with the restless legs syndrome (RLS) is established in humans and was reported in spinal cord injury (SCI) patients classified by the American Spinal Injury Association (ASIA) as A. Its pathogenesis has not been completely unraveled, though recent advances might enhance our knowledge about those malfunctions. PLM...

Date: 2012   |   Origin: Oasisbr

The review of the methods to obtain non-neuronal cells to study glial influence...

Scorisa,Juliana Milani; Duobles,Tatiana; de Oliveira,Gabriela Pintar; Maximino,Jessica Ruivo; Chadi,Gerson

PURPOSE: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that displays a rapid evolution. Current treatments have failed to revert clinical symptoms because the mechanisms involved in the death of motoneuron are still unknown. Recent publications have put non-neuronal cells, particularly, astrocyte and microglia, in the scenario of pathophisiology of the disease. Animal models for ALS, ...

Date: 2010   |   Origin: Oasisbr

S100ß and fibroblast growth factor-2 are present in cultured Schwann cells and ...

Duobles,Tatiana; Lima,Thais de Sousa; Levy,Beatriz de Freitas Azevedo; Chadi,Gerson

PURPOSE: The neurotrophic factor fibroblast growth factor-2 (FGF-2, bFGF) and Ca++ binding protein S100ß are expressed by the Schwann cells of the peripheral nerves and by the satellite cells of the dorsal root ganglia (DRG). Recent studies have pointed out the importance of the molecules in the paracrine mechanisms related to neuronal maintenance and plasticity of lesioned motor and sensory peripheral neurons....

Date: 2008   |   Origin: Oasisbr

Differential astroglial responses in the spinal cord of rats submitted to a sci...

Dallo,João Gabriel Martins; Reichert,Bernardo Vergara; Valladão Júnior,José Benedito Ramos; Silva,Camila; Luca,Bianca Aparecida de

PURPOSE: Reactive astrocytes are implicated in several mechanisms after central or peripheral nervous system lesion, including neuroprotection, neuronal sprouting, neurotransmission and neuropathic pain. Schwann cells (SC), a peripheral glia, also react after nerve lesion favoring wound/repair, fiber outgrowth and neuronal regeneration. We investigated herein whether cell therapy for repair of lesioned sciatic ...

Date: 2007   |   Origin: Oasisbr

Striatal injection of 6-hydroxydopamine induces retrograde degeneration and gli...

Rodrigues,Ricardo Wilson Pinho; Gomide,Vânia Canterucci; Chadi,Gerson

PURPOSE: The effect of a highly selective 6-hydroxydopamine (6-OHDA)-induced lesion of the nigrostriatal system on the astroglial and microglial activation was analysed in adult Wistar rats after an unilateral striatal injection of the neurotoxin. METHODS: Male rats received an unilateral stereotaxical injection of the 6-OHDA in the left side of the neostriatum and were sacrificed 22 days later. Control animals...

Date: 2003   |   Origin: Oasisbr

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