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Chloroquine-induced myopathy

Lupus, 2011-06, Vol.20 (7), p.773-774

2011

Volltextzugriff (PDF)

Myoadenylate deaminase deficiency: clinico-pathological and molecular study of a series of 27 Spanish cases

Clinical neuropathology, 2009-03, Vol.28 (2), p.136

2009

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LGMD1F: A morphological study

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S236-S236

2015

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Light-chain-restricted germinal centres in reactive lymphadenitis: report of eight cases

Histopathology, 2008-03, Vol.52 (4), p.436-444

2008

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Late-onset sporadic nemaline myopathy presenting as hypercapnic respiratory failure

Neurología (Barcelona, English ed. ), 2024-01, Vol.39 (1), p.99-101

2024

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P.156 Novel repeat expansions in PLIN4 in two Spanish families suffering from autosomal dominant distal myopathy with unique pathological features

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S110

2022

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M.P.2.11 Morphological studies in an eleven week-gestation foetus with glycogenosis II (Pompe disease)

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.796-796

2007

Volltextzugriff (PDF)

G.P.13.16 Vacuolar myopathies. A morphological approach

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.853-853

2007

Volltextzugriff (PDF)

Diplopía aislada como forma de presentación de CADASIL: a propósito de un caso

Neurología (Barcelona, Spain), 2014-01, Vol.29 (1), p.56-59

2014

Volltextzugriff (PDF)

Isolated diplopia as a form of presentation of CADASIL: presentation of a case

Neurologia (Barcelona, Spain), 2014-01, Vol.29 (1), p.56

2014

Volltextzugriff (PDF)

P.303 - Variable skeletal muscle involvement in VARS2 mitochondrial encephalomyopathy

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S178-S178

2016

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P.120EUROMAC: A European registry for patients with McArdle disease and other very rare muscle glycogenoses

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S83-S83

2019

Volltextzugriff (PDF)

G.P.171 - LGMD1F: A morphological study

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S236-S236

2015

Volltextzugriff (PDF)

Variable skeletal muscle involvement in VARS2 mitochondrial encephalomyopathy

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S178-S178

2016

Volltextzugriff (PDF)

P3.23 Characterization of a new mutation in the GADP1 gene causing axonal autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.688-689

2011

Volltextzugriff (PDF)

Behavioural variant of frontotemporal dementia as the presenting symptom of corticobasal degeneration

Revista de neurologiá, 2018-12, Vol.67 (11), p.436-440

2018

Volltextzugriff (PDF)

G.P.16.05. McArdle disease. Molecular study of the myophosphorylase gene (PYGM) in a series of 120 patients

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.828-828

2008

Volltextzugriff (PDF)

P3.4 Spinal muscular atrophy with respiratory distress type 1 (SMARD-1). A clinico-pathological follow-up

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.683-683

2011

Volltextzugriff (PDF)

MIOPATÍA NEMALINICA ESPORADICA DE INICIO TARDIO MANIFESTANDOSE COMO UNA INSUFICIENCIA RESPIRATORIA HIPERCAPNICA

Neurología (Barcelona, Spain), 2024-01, Vol.39 (1), p.99-101

2024

Volltextzugriff (PDF)

Isolated diplopia as a form of presentation of CADASIL: Presentation of a case

Neurología (Barcelona, English ed. ), 2014-01, Vol.29 (1), p.56-59

2014

Volltextzugriff (PDF)

Multicentric Reticulohistiocytosis Treated Successfully with Etanercept

The open dermatology journal, 2008-05, Vol.2 (1), p.44-47

2008

Volltextzugriff (PDF)

Miopatía por deficiencia de mioadenilato desaminasa desencadenada por el tratamiento con atorvastatina

Medicina clínica, 2013-06, Vol.140 (12), p.565-567

2013

Volltextzugriff (PDF)

Improving the Outcomes of Organs Obtained From Controlled Donation After Circulatory Death Donors Using Abdominal Normothermic Regional Perfusion

American journal of transplantation, 2017-08, Vol.17 (8), p.2165-2172

2017

Volltextzugriff (PDF)

Positive selection and compensatory adaptation interact to stabilize non-transmissible plasmids

Nature communications, 2014-10, Vol.5 (1), p.5208-5208, Article 5208

2014

Volltextzugriff (PDF)

Chloroquine-induced myopathy

Lupus, 2011, Vol.20 (7), p.773-774

2011

Volltextzugriff (PDF)

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Chloroquine-induced myopathy

Myoadenylate deaminase deficiency: clinico-pathological and molecular study of a series of 27 Spanish cases

LGMD1F: A morphological study

Light-chain-restricted germinal centres in reactive lymphadenitis: report of eight cases

Late-onset sporadic nemaline myopathy presenting as hypercapnic respiratory failure

P.156 Novel repeat expansions in PLIN4 in two Spanish families suffering from autosomal dominant distal myopathy with unique pathological features

M.P.2.11 Morphological studies in an eleven week-gestation foetus with glycogenosis II (Pompe disease)

G.P.13.16 Vacuolar myopathies. A morphological approach

Diplopía aislada como forma de presentación de CADASIL: a propósito de un caso

Isolated diplopia as a form of presentation of CADASIL: presentation of a case

P.303 - Variable skeletal muscle involvement in VARS2 mitochondrial encephalomyopathy

P.120EUROMAC: A European registry for patients with McArdle disease and other very rare muscle glycogenoses

G.P.171 - LGMD1F: A morphological study

Variable skeletal muscle involvement in VARS2 mitochondrial encephalomyopathy

P3.23 Characterization of a new mutation in the GADP1 gene causing axonal autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

Behavioural variant of frontotemporal dementia as the presenting symptom of corticobasal degeneration

G.P.16.05. McArdle disease. Molecular study of the myophosphorylase gene (PYGM) in a series of 120 patients

P3.4 Spinal muscular atrophy with respiratory distress type 1 (SMARD-1). A clinico-pathological follow-up

MIOPATÍA NEMALINICA ESPORADICA DE INICIO TARDIO MANIFESTANDOSE COMO UNA INSUFICIENCIA RESPIRATORIA HIPERCAPNICA

Isolated diplopia as a form of presentation of CADASIL: Presentation of a case

Multicentric Reticulohistiocytosis Treated Successfully with Etanercept

Miopatía por deficiencia de mioadenilato desaminasa desencadenada por el tratamiento con atorvastatina

Improving the Outcomes of Organs Obtained From Controlled Donation After Circulatory Death Donors Using Abdominal Normothermic Regional Perfusion

Positive selection and compensatory adaptation interact to stabilize non-transmissible plasmids

Chloroquine-induced myopathy

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