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The scatter factor signaling pathways as therapeutic associated target in cancer treatment

Current medicinal chemistry, 2010-09, Vol.17 (25), p.2699

2010

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Primary Headaches in Children: Clinical Findings and the Association with other Conditions

International journal of immunopathology and pharmacology, 2012-10, Vol.25 (4), p.1083-1091

2012

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Stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements

Frontiers in neuroengineering, 2012, Vol.5, p.12-12

2012

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Acquired Peripheral Neuropathy: A Report on 20 Children

International journal of immunopathology and pharmacology, 2012-04, Vol.25 (2), p.513-517

2012

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Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis

Neuropediatrics, 2010-12, Vol.41 (6), p.246

2010

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Temporal summation of the nociceptive withdrawal reflex involves deactivation of posterior cingulate cortex

European journal of pain, 2017-02, Vol.21 (2), p.289-301

2017

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Pontocerebellar hypoplasia: clinical, pathologic, and genetic studies

Neurology, 2010-10, Vol.75 (16), p.1459

2010

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Earliest clinical manifestations and natural history of neurofibromatosis type 2 (NF2) in childhood: a study of 24 patients

Neuropediatrics, 2005-02, Vol.36 (1), p.21

2005

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Krabbe leukodystrophy in a selected population with high rate of late onset forms: longer survival linked to c.121G>A (p.Gly41Ser) mutation

Clinical genetics, 2011-11, Vol.80 (5), p.452-458

2011

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Neurological manifestations in individuals with pure cutaneous or syndromic (Ruggieri-Happle syndrome) phenotypes with "cutis tricolor": a study of 14 cases

Neuropediatrics, 2010-08, Vol.41 (2), p.60

2010

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Mapping, cloning and genetic characterization of the region containing the Wilson disease gene

Nature genetics, 1993-12, Vol.5 (4), p.338-343

1993

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High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy

Clinical genetics, 2012-09, Vol.82 (3), p.277-282

2012

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Multiple sclerosis in children under 10 years of age

Neurological sciences, 2004-11, Vol.25 Suppl 4 (S4), p.S326-s335

2004

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Comparison of different tissue sampling for PCR-based diagnosis and follow-up of canine visceral leishmaniosis

Veterinary parasitology, 2004-11, Vol.125 (3), p.251-262

2004

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The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

Nature genetics, 1993-12, Vol.5 (4), p.344-350

1993

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PA13 THE NEUROLOGY OF COELIAC DISEASE IN CHILDHOOD: WHAT IS THE EVIDENCE? A SYSTEMATIC REVIEW AND META-ANALYSIS

Digestive and liver disease, 2010, Vol.42, p.S347-S347

2010

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Role of the serotonin transporter in heart valve development and disease

Veterinary research communications, 2009-09, Vol.33 (Suppl 1), p.117-119

2009

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Natural killer cell cytotoxicity is enhanced by very low doses of rIL-2 and rIFN-α in patients with renal cell carcinoma

Medical oncology (Northwood, London, England), 2009-03, Vol.26 (1), p.38-44

2009

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Expression of the serotonin transporter (SERT) gene during mouse development

Veterinary research communications, 2008-09, Vol.32 (Suppl 1), p.167-169

2008

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Headache in paediatric patients with celiac disease and its prevalence as a diagnostic clue

Digestive and liver disease, 2008, Vol.40 (10), p.A86-A86

2008

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Peripheral neuropathy in Wegener’s granulomatosis, Churg–Strauss syndrome and microscopic polyangiitis

Journal of neurology, neurosurgery and psychiatry, 2007-10, Vol.78 (10), p.1119-1123

2007

Volltextzugriff (PDF)

T1-WEIGHTED BRAIN MRI: QUALITY ASSESSMENT, VARIABILITY AND REPRODUCIBILITY OF ANATOMICAL MEASUREMENTS IN THE RIN–NEUROIMAGING NETWORK

Physica medica, 2023-11, Vol.115, p.102753, Article 102753

2023

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ENT Wegener's granulomatosis can hide severe central nervous system involvement

Clinical rheumatology, 2005-06, Vol.24 (3), p.290-293

2005

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Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD

Neuromuscular disorders : NMD, 2002-10, Vol.12 (7), p.623-630

2002

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Clinical and neuroradiological follow-up in mucopolysaccharidosis type III (Sanfilippo syndrome)

Neuropediatrics, 1999-10, Vol.30 (5), p.270

1999

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The scatter factor signaling pathways as therapeutic associated target in cancer treatment

Primary Headaches in Children: Clinical Findings and the Association with other Conditions

Stop-event-related potentials from intracranial electrodes reveal a key role of premotor and motor cortices in stopping ongoing movements

Acquired Peripheral Neuropathy: A Report on 20 Children

Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis

Temporal summation of the nociceptive withdrawal reflex involves deactivation of posterior cingulate cortex

Pontocerebellar hypoplasia: clinical, pathologic, and genetic studies

Earliest clinical manifestations and natural history of neurofibromatosis type 2 (NF2) in childhood: a study of 24 patients

Krabbe leukodystrophy in a selected population with high rate of late onset forms: longer survival linked to c.121G>A (p.Gly41Ser) mutation

Neurological manifestations in individuals with pure cutaneous or syndromic (Ruggieri-Happle syndrome) phenotypes with "cutis tricolor": a study of 14 cases

Mapping, cloning and genetic characterization of the region containing the Wilson disease gene

High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy

Multiple sclerosis in children under 10 years of age

Comparison of different tissue sampling for PCR-based diagnosis and follow-up of canine visceral leishmaniosis

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

PA13 THE NEUROLOGY OF COELIAC DISEASE IN CHILDHOOD: WHAT IS THE EVIDENCE? A SYSTEMATIC REVIEW AND META-ANALYSIS

Role of the serotonin transporter in heart valve development and disease

Natural killer cell cytotoxicity is enhanced by very low doses of rIL-2 and rIFN-α in patients with renal cell carcinoma

Expression of the serotonin transporter (SERT) gene during mouse development

Headache in paediatric patients with celiac disease and its prevalence as a diagnostic clue

Peripheral neuropathy in Wegener’s granulomatosis, Churg–Strauss syndrome and microscopic polyangiitis

T1-WEIGHTED BRAIN MRI: QUALITY ASSESSMENT, VARIABILITY AND REPRODUCIBILITY OF ANATOMICAL MEASUREMENTS IN THE RIN–NEUROIMAGING NETWORK

ENT Wegener's granulomatosis can hide severe central nervous system involvement

Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD

Clinical and neuroradiological follow-up in mucopolysaccharidosis type III (Sanfilippo syndrome)

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