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CSF characteristics in early-onset multiple sclerosis

Neurology, 2004-11, Vol.63 (10), p.1966

2004

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High seroprevalence of Epstein-Barr virus in children with multiple sclerosis

Neurology, 2006-12, Vol.67 (11), p.2063

2006

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Quantitative proton MRS of Pelizaeus-Merzbacher disease: evidence of dys- and hypomyelination

Neurology, 2005-09, Vol.65 (5), p.701

2005

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MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin

American journal of human genetics, 2001-05, Vol.68 (5), p.1093-1101

2001

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Paediatric and adult multiple sclerosis: age-related differences and time course of the neuroimmunological response in cerebrospinal fluid

Multiple sclerosis, 2009-12, Vol.15 (12), p.1466-1480

2009

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Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients

Human molecular genetics, 2000-05, Vol.9 (9), p.1369-1375

2000

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Pediatric multiple sclerosis – a short history of a long story

European journal of paediatric neurology, 2008, Vol.12, p.S12-S12

Hanefeld, F

2008

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X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene

Journal of neurology, 2005-06, Vol.252 (6), p.663-666

2005

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Proton MRS profile of cerebral metabolic abnormalities in Krabbe disease

Neurology, 2003-03, Vol.60 (5), p.819

2003

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Increase of total creatine in human brain after oral supplementation of creatine-monohydrate

American journal of physiology. Regulatory, integrative and comparative physiology, 1999-09, Vol.277 (3), p.698-R704

1999

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Intrathecal IgM synthesis in pediatric MS is not a negative prognostic marker of disease progression: quantitative versus qualitative IgM analysis

Multiple sclerosis, 2011-03, Vol.17 (3), p.327-334

2011

Volltextzugriff (PDF)

Baló’s concentric sclerosis associated with primary human herpesvirus 6 infection

Journal of neurology, neurosurgery and psychiatry, 2005-12, Vol.76 (12), p.1723-1725

2005

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Creatine deficiency in the brain : a new, treatable inborn error of metabolism

Pediatric research, 1994-09, Vol.36 (3), p.409-413

1994

Volltextzugriff (PDF)

Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regions

Human mutation, 2001-03, Vol.17 (3), p.183-190

2001

Volltextzugriff (PDF)

Alexander disease: past and present

Cellular and molecular life sciences : CMLS, 2004-11, Vol.61 (21), p.2750-2752

Hanefeld, F A

2004

Volltextzugriff (PDF)

Guanidinoacetate methyltransferase deficiency : The first inborn error of creatine metabolism in man

American journal of human genetics, 1996-05, Vol.58 (5), p.914-922

1996

Volltextzugriff (PDF)

Proton MRS of a child with Sandhoff disease reveals elevated brain hexosamine

European journal of paediatric neurology, 2008-01, Vol.12 (1), p.56-60

2008

Volltextzugriff (PDF)

Quantitative proton magnetic resonance spectroscopy of childhood adrenoleukodystrophy

Neuropediatrics, 1998-10, Vol.29 (5), p.254

1998

Volltextzugriff (PDF)

Chronic relapsing opsoclonus-myoclonus syndrome: Combination of cyclophosphamide and dexamethasone pulses

European journal of paediatric neurology, 2008-01, Vol.12 (1), p.51-55

2008

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Foix–Chavany–Marie (anterior operculum) syndrome in childhood: a reappraisal of Worster-Drought syndrome

Developmental medicine and child neurology, 2000-02, Vol.42 (2), p.122-132, Article S0012162200000232

2000

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Clinical and genetic heterogeneity in megalencephalic leukoencephalopathy with subcortical cysts (MLC)

Neuropediatrics, 2003-08, Vol.34 (4), p.215

2003

Volltextzugriff (PDF)

Pediatric multiple sclerosis: a short history of a long story

Neurology, 2007-04, Vol.68 (16 Suppl 2), p.S3

Hanefeld, Folker

2007

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Influence of mutation type and location on phenotype in 123 patients with Rett syndrome

Neuropediatrics, 2002-04, Vol.33 (2), p.63

2002

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Quantitative proton magnetic resonance spectroscopy of children with adrenoleukodystrophy before and after hematopoietic stem cell transplantation

Neuropediatrics, 2003-10, Vol.34 (5), p.237

2003

Volltextzugriff (PDF)

MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution

Journal of medical genetics, 2002-08, Vol.39 (8), p.586-588

2002

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CSF characteristics in early-onset multiple sclerosis

High seroprevalence of Epstein-Barr virus in children with multiple sclerosis

Quantitative proton MRS of Pelizaeus-Merzbacher disease: evidence of dys- and hypomyelination

MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin

Paediatric and adult multiple sclerosis: age-related differences and time course of the neuroimmunological response in cerebrospinal fluid

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients

Pediatric multiple sclerosis – a short history of a long story

X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene

Proton MRS profile of cerebral metabolic abnormalities in Krabbe disease

Increase of total creatine in human brain after oral supplementation of creatine-monohydrate

Intrathecal IgM synthesis in pediatric MS is not a negative prognostic marker of disease progression: quantitative versus qualitative IgM analysis

Baló’s concentric sclerosis associated with primary human herpesvirus 6 infection

Creatine deficiency in the brain : a new, treatable inborn error of metabolism

Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regions

Alexander disease: past and present

Guanidinoacetate methyltransferase deficiency : The first inborn error of creatine metabolism in man

Proton MRS of a child with Sandhoff disease reveals elevated brain hexosamine

Quantitative proton magnetic resonance spectroscopy of childhood adrenoleukodystrophy

Chronic relapsing opsoclonus-myoclonus syndrome: Combination of cyclophosphamide and dexamethasone pulses

Foix–Chavany–Marie (anterior operculum) syndrome in childhood: a reappraisal of Worster-Drought syndrome

Clinical and genetic heterogeneity in megalencephalic leukoencephalopathy with subcortical cysts (MLC)

Pediatric multiple sclerosis: a short history of a long story

Influence of mutation type and location on phenotype in 123 patients with Rett syndrome

Quantitative proton magnetic resonance spectroscopy of children with adrenoleukodystrophy before and after hematopoietic stem cell transplantation

MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution

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