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MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2

Brain (London, England : 1878), 2006-08, Vol.129 (8), p.2093-2102

2006

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Lyme Neuroborreliosis in Children

Annals of medicine (Helsinki), 1996, Vol.28 (3), p.235-240

Christen, Hans-Jurgen

1996

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Mutations in the β-tropomyosin ( TPM2) gene – a rare cause of nemaline myopathy

Neuromuscular disorders : NMD, 2002-02, Vol.12 (2), p.151-158

2002

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Ullrich congenital muscular dystrophy: Connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromes

American journal of medical genetics, 2005-01, Vol.132A (3), p.296-301

2005

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Endocrinological study on growth retardation in Rett syndrome

Acta Paediatrica, 2001-11, Vol.90 (11), p.1257-1261

2001

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Primarily chronic and cerebrovascular course of Lyme neuroborreliosis: case reports and literature review

Archives of disease in childhood, 2000-07, Vol.83 (1), p.67-71

2000

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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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Otogene und sinugene intrakranielle Komplikationen bei Kindern – eine interdisziplinäre Herausforderung

Laryngo-Rhino-Otologie, 2004

2004

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A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndrome

Neuromuscular disorders : NMD, 2004-11, Vol.14 (11), p.744-749

2004

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Acute peripheral facial palsy in Lyme disease -- a distal neuritis at the infection site

Neuropediatrics, 2004-10, Vol.35 (5), p.267

2004

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Treatment of apneustic respiratory disturbance with a serotonin-receptor agonist

The Journal of pediatrics, 1997, Vol.130 (1), p.89-94

1997

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Autoantibodies to human manganese superoxide dismutase (MnSOD) in children with facial palsy due to neuroborreliosis

Neuropediatrics, 2005-12, Vol.36 (6), p.386

2005

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Nondifferentiation between Lyme disease spirochetes from vector ticks and human cerebrospinal fluid

The Journal of infectious diseases, 1995-02, Vol.171 (2), p.476

1995

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Treatment of primary malignant rhabdoid tumor of the brain: report of three cases and review of the literature

International journal of radiation oncology, biology, physics, 1998-07, Vol.41 (5), p.1013-1019

1998

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Otogene und sinugene intrakranielle Komplikationen bei Kindern – eine interdisziplinäre Herausforderung

Laryngo- rhino- otologie, 2004-02, Vol.83 (2)

2004

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Etiology of the Acrodermatitis Chronica Atrophicans Lesion in Lyme Disease

The Journal of infectious diseases, 1996-08, Vol.174 (2), p.421-423

1996

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Alterations of brain metabolites in metachromatic leukodystrophy as detected by localized proton magnetic resonance spectroscopy in vivo

Journal of neurology, 1993-12, Vol.241 (2), p.68-74

1993

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Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA : A clinical and molecular genetic study of four children with Kearns-Sayre syndrome

Pediatric research, 1997-02, Vol.41 (2), p.193-200

1997

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Potential prognostic value of C-erbB-2 expression in medulloblastomas in very young children

Journal of pediatric hematology/oncology, 1997-11, Vol.19 (6), p.510-515

1997

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Immunohistochemistry of primary central nervous system malignant rhabdoid tumors : report of five cases and review of the literature

Acta neuropathologica, 1996, Vol.91 (6), p.578-586

1996

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Lyme borreliosis in childhood

HNO, 1995-08, Vol.43 (8), p.507-519

1995

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Evaluation of the polymerase chain reaction for the detection of Borrelia burgdorferi in cerebrospinal fluid of children with acute peripheral facial palsy

European journal of pediatrics, 1995-05, Vol.154 (5), p.374-377

1995

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Multiple sclerosis in childhood: Report of 15 cases

Brain & development (Tokyo. 1979), 1991-11, Vol.13 (6), p.410-416

1991

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Fatal Pseudallescheria boydii panencephalitis in a child after near-drowning

The Pediatric infectious disease journal, 1996-04, Vol.15 (4), p.365-370

1996

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Aplasia of the depressor anguli oris muscle: a rare cause of congenital lower lip palsy?

Neuropediatrics, 1998-08, Vol.29 (4), p.215

1998

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MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2

Lyme Neuroborreliosis in Children

Mutations in the β-tropomyosin ( TPM2) gene – a rare cause of nemaline myopathy

Ullrich congenital muscular dystrophy: Connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromes

Endocrinological study on growth retardation in Rett syndrome

Primarily chronic and cerebrovascular course of Lyme neuroborreliosis: case reports and literature review

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

Otogene und sinugene intrakranielle Komplikationen bei Kindern – eine interdisziplinäre Herausforderung

A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndrome

Acute peripheral facial palsy in Lyme disease -- a distal neuritis at the infection site

Treatment of apneustic respiratory disturbance with a serotonin-receptor agonist

Autoantibodies to human manganese superoxide dismutase (MnSOD) in children with facial palsy due to neuroborreliosis

Nondifferentiation between Lyme disease spirochetes from vector ticks and human cerebrospinal fluid

Treatment of primary malignant rhabdoid tumor of the brain: report of three cases and review of the literature

Otogene und sinugene intrakranielle Komplikationen bei Kindern – eine interdisziplinäre Herausforderung

Etiology of the Acrodermatitis Chronica Atrophicans Lesion in Lyme Disease

Alterations of brain metabolites in metachromatic leukodystrophy as detected by localized proton magnetic resonance spectroscopy in vivo

Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA : A clinical and molecular genetic study of four children with Kearns-Sayre syndrome

Potential prognostic value of C-erbB-2 expression in medulloblastomas in very young children

Immunohistochemistry of primary central nervous system malignant rhabdoid tumors : report of five cases and review of the literature

Lyme borreliosis in childhood

Evaluation of the polymerase chain reaction for the detection of Borrelia burgdorferi in cerebrospinal fluid of children with acute peripheral facial palsy

Multiple sclerosis in childhood: Report of 15 cases

Fatal Pseudallescheria boydii panencephalitis in a child after near-drowning

Aplasia of the depressor anguli oris muscle: a rare cause of congenital lower lip palsy?

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