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Fever after intraventricular neuroendoscopic procedures in children

Child's nervous system, 2016-06, Vol.32 (6), p.1049-1055

2016

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rhGGF2 protects against cisplatin-induced neuropathy in the rat

Journal of neuroscience research, 2000-04, Vol.60 (2), p.237-244

2000

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Armoured brain: case report of a symptomatic calcified chronic subdural haematoma

Journal of neurology, neurosurgery and psychiatry, 2007-05, Vol.78 (5), p.542-543

2007

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Neuronal Ca2+ disregulation in diabetes mellitus

European journal of pharmacology, 2002-07, Vol.447 (2-3), p.201-209

2002

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The potent melanocortin receptor agonist melanotan-II promotes peripheral nerve regeneration and has neuroprotective properties in the rat

European journal of pharmacology, 2003-02, Vol.462 (1), p.179-183

2003

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rhGGF2 Protects Against Cisplatin-Induced Neuropathy in the Rat

Journal of neuroscience research, 2000-04, Vol.60 (2), p.237-244

2000

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Are psychosocial factors, risk factors for symptoms and signs of the shoulder, elbow, or hand/wrist?: A review of the epidemiological literature

American journal of industrial medicine, 2002-05, Vol.41 (5), p.315-342

2002

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COGNITIVE AND MOTOR IMPROVEMENTS AFTER RECONSTRUCTION OF LARGE SKULL DEFECTS USING PATIENT SPECIFIC IMPLANTS

International journal of oral and maxillofacial surgery, 2024-01, Vol.52, p.163

2024

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P057 - COGNITIVE AND MOTOR IMPROVEMENTS AFTER RECONSTRUCTION OF LARGE SKULL DEFECTS USING PATIENT SPECIFIC IMPLANTS

International journal of oral and maxillofacial surgery, 2024-01, Vol.52, p.163-163

2024

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Clinical characteristics of type 1 diabetic patients with and without severe hypoglycemia

Diabetes care, 2000-10, Vol.23 (10), p.1467-1471

2000

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Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?

Neurology, 2008-05, Vol.70 (20), p.1876-1882

2008

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The therapeutic effect of patient-specific implants in cranioplasty

International journal of oral and maxillofacial surgery, 2017-03, Vol.46, p.208-208

2017

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Multiple oxidative phosphorylation deficiencies in severe childhood multi-system disorders due to polymerase gamma (POLGI) mutations

European journal of pediatrics, 2007-03, Vol.166 (3), p.229-234

2007

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A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core‐like lesions

Brain (London, England : 1878), 2003-07, Vol.126 (7), p.1545-1551

2003

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Neuromuscular abnormalities in ataxia telangiectasia: a clinical, electrophysiological and muscle ultrasound study

Neuropediatrics, 2007-06, Vol.38 (3), p.117-121

2007

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Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia

Neurology, 2006-07, Vol.67 (2), p.346-349

2006

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Solution structure of the receptor tyrosine kinase EphB2 SAM domain and identification of two distinct homotypic interaction sites

Protein science, 1999-10, Vol.8 (10), p.1954-1961

1999

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Implementation of a mobile 0.15-T intraoperative MR system in pediatric neuro-oncological surgery: feasibility and correlation with early postoperative high-field strength MRI

Child's nervous system, 2012-08, Vol.28 (8), p.1171-1180

2012

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Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle

Journal of neurology, 2007-11, Vol.254 (11), p.1614-1615

2007

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Muscle-fiber conduction velocity and electromyography as diagnostic tools in patients with suspected inflammatory myopathy: A prospective study

Muscle & nerve, 2004-01, Vol.29 (1), p.46-50

2004

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Genetic characteristics of myoadenylate deaminase deficiency

Annals of neurology, 1998-07, Vol.44 (1), p.140-143

1998

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Intramedullary cavernoma presenting with hematomyelia: report of two girls

Child's nervous system, 2010-03, Vol.26 (3), p.391-398

2010

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Muscle 3243A→G mutation load and capacity of the mitochondrial energy-generating system

Annals of neurology, 2008-04, Vol.63 (4), p.473-481

2008

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Deficiency of the voltage-dependent anion channel : A novel cause of mitochondriopathy

Pediatric research, 1996-05, Vol.39 (5), p.760-765

1996

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Lipophilicity and hydrogen-bonding capacity of H1-antihistaminic agents in relation to their central sedative side-effects

European journal of pharmaceutical sciences, 1994-12, Vol.2 (5-6), p.373-384

1994

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Fever after intraventricular neuroendoscopic procedures in children

rhGGF2 protects against cisplatin-induced neuropathy in the rat

Armoured brain: case report of a symptomatic calcified chronic subdural haematoma

Neuronal Ca2+ disregulation in diabetes mellitus

The potent melanocortin receptor agonist melanotan-II promotes peripheral nerve regeneration and has neuroprotective properties in the rat

rhGGF2 Protects Against Cisplatin-Induced Neuropathy in the Rat

Are psychosocial factors, risk factors for symptoms and signs of the shoulder, elbow, or hand/wrist?: A review of the epidemiological literature

COGNITIVE AND MOTOR IMPROVEMENTS AFTER RECONSTRUCTION OF LARGE SKULL DEFECTS USING PATIENT SPECIFIC IMPLANTS

P057 - COGNITIVE AND MOTOR IMPROVEMENTS AFTER RECONSTRUCTION OF LARGE SKULL DEFECTS USING PATIENT SPECIFIC IMPLANTS

Clinical characteristics of type 1 diabetic patients with and without severe hypoglycemia

Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?

The therapeutic effect of patient-specific implants in cranioplasty

Multiple oxidative phosphorylation deficiencies in severe childhood multi-system disorders due to polymerase gamma (POLGI) mutations

A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core‐like lesions

Neuromuscular abnormalities in ataxia telangiectasia: a clinical, electrophysiological and muscle ultrasound study

Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia

Solution structure of the receptor tyrosine kinase EphB2 SAM domain and identification of two distinct homotypic interaction sites

Implementation of a mobile 0.15-T intraoperative MR system in pediatric neuro-oncological surgery: feasibility and correlation with early postoperative high-field strength MRI

Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle

Muscle-fiber conduction velocity and electromyography as diagnostic tools in patients with suspected inflammatory myopathy: A prospective study

Genetic characteristics of myoadenylate deaminase deficiency

Intramedullary cavernoma presenting with hematomyelia: report of two girls

Muscle 3243A→G mutation load and capacity of the mitochondrial energy-generating system

Deficiency of the voltage-dependent anion channel : A novel cause of mitochondriopathy

Lipophilicity and hydrogen-bonding capacity of H1-antihistaminic agents in relation to their central sedative side-effects

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