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Cerebral Sinovenous Thrombosis in Children

The New England journal of medicine, 2001-08, Vol.345 (6), p.417-423

2001

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Autoantibodies in childhood post-varicella acute cerebellar ataxia

Canadian journal of neurological sciences, 2000-11, Vol.27 (4), p.316-320

2000

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Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1

Nature genetics, 2001-09, Vol.29 (1), p.75-77

2001

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Comparison of conventional and non-invasive techniques for the early identification of diabetic neuropathy in children and adolescents with type 1 diabetes

Pediatric diabetes, 2006-12, Vol.7 (6), p.305-310

2006

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Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)

Annals of neurology, 2003-12, Vol.54 (6), p.719-724

2003

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Congenital autosomal dominant distal spinal muscular atrophy

Neuromuscular disorders : NMD, 1998-08, Vol.8 (6), p.405-408

1998

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autosomal recessive cerebellar hypoplasia in the hutterite population

Developmental medicine and child neurology, 2005-10, Vol.47 (10), p.691-695

2005

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PEDIATRIC CLINICAL ELECTROMYOGRAPHY. 1996. By Royden JonesJr. , Charles F. Bolton and C. Michel HarperJr. . Published by Lippincott-Raven. 487 pages. $C127.00

Canadian journal of neurological sciences, 1997-02, Vol.24 (1), p.175-176

Adams, Coleen

1997

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Autosomal recessive cerebellar hypoplasia in the Hutterite population

Developmental medicine and child neurology, 2005-10, Vol.47 (10), p.691-695

2005

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Severe infantile axonal neuropathy with respiratory failure

Muscle & nerve, 2001-06, Vol.24 (6), p.760-768

2001

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Sleep-disordered breathing in Duchenne muscular dystrophy: A preliminary study of the role of portable monitoring

Pediatric pulmonology, 2000-02, Vol.29 (2), p.135-140

2000

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INTERNATIONAL HEADACHE SOCIETY CRITERIA AND CHILDHOOD HEADACHE

Developmental medicine and child neurology, 1994-05, Vol.36 (5), p.419-428

1994

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Neuromuscular complications of bone marrow transplantation

Pediatric neurology, 1995-01, Vol.12 (1), p.58-61

1995

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Mutations in the gene encoding immunoglobulin [mu]-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1

Nature genetics, 2001-09, Vol.29 (1), p.75

2001

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Middle cerebral artery dissection

Neuropediatrics, 1996-12, Vol.27 (6), p.331-332

1996

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Mutations in the gene encoding immunoglobulin k-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1

Nature genetics, 2001-09, Vol.29 (1), p.75-77

2001

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Thymectomy in Juvenile Myasthenia Gravis

Journal of child neurology, 1990-07, Vol.5 (3), p.215-218

1990

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Comparison of SPECT, EEG, CT, MRI, and pathology in partial epilepsy

Pediatric neurology, 1992-03, Vol.8 (2), p.97-103

1992

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Chiasmal glioma in neurofibromatosis type 1 with severe visual loss regained with radiation

Pediatric neurology, 1997-07, Vol.17 (1), p.80-82

1997

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Acute transverse myelopathy in children

Canadian journal of neurological sciences, 1990-02, Vol.17 (1), p.40-45

1990

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Primary hypothyroidism with intracranial hypertension and pituitary hyperplasia

Pediatric neurology, 1994-03, Vol.10 (2), p.166-168

1994

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Inter-Observer Agreement in the Diagnosis of Childhood Headache

Headache, 1994-09, Vol.34 (8), p.467-470

1994

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International headache society (IHS) criteria and childhood headache

Pediatric neurology, 1992-09, Vol.8 (5), p.371-371

1992

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Late‐onset Hexosaminidase A and Hexosaminidase A and B Deficiency: Family Study and Review

Developmental medicine and child neurology, 1986-04, Vol.28 (2), p.236-243

1986

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Primary thalamic and caudate hemorrhage in term neonates presenting with seizures

Pediatric neurology, 1988-05, Vol.4 (3), p.175-177

1988

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Cerebral Sinovenous Thrombosis in Children

Autoantibodies in childhood post-varicella acute cerebellar ataxia

Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1

Comparison of conventional and non-invasive techniques for the early identification of diabetic neuropathy in children and adolescents with type 1 diabetes

Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)

Congenital autosomal dominant distal spinal muscular atrophy

autosomal recessive cerebellar hypoplasia in the hutterite population

PEDIATRIC CLINICAL ELECTROMYOGRAPHY. 1996. By Royden JonesJr. , Charles F. Bolton and C. Michel HarperJr. . Published by Lippincott-Raven. 487 pages. $C127.00

Autosomal recessive cerebellar hypoplasia in the Hutterite population

Severe infantile axonal neuropathy with respiratory failure

Sleep-disordered breathing in Duchenne muscular dystrophy: A preliminary study of the role of portable monitoring

INTERNATIONAL HEADACHE SOCIETY CRITERIA AND CHILDHOOD HEADACHE

Neuromuscular complications of bone marrow transplantation

Mutations in the gene encoding immunoglobulin [mu]-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1

Middle cerebral artery dissection

Mutations in the gene encoding immunoglobulin k-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1

Thymectomy in Juvenile Myasthenia Gravis

Comparison of SPECT, EEG, CT, MRI, and pathology in partial epilepsy

Chiasmal glioma in neurofibromatosis type 1 with severe visual loss regained with radiation

Acute transverse myelopathy in children

Primary hypothyroidism with intracranial hypertension and pituitary hyperplasia

Inter-Observer Agreement in the Diagnosis of Childhood Headache

International headache society (IHS) criteria and childhood headache

Late‐onset Hexosaminidase A and Hexosaminidase A and B Deficiency: Family Study and Review

Primary thalamic and caudate hemorrhage in term neonates presenting with seizures

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