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Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

Nature genetics, 1998-04, Vol.18 (4), p.382-384

1998

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Functional Consequences of Mutations in the Early Growth Response 2 Gene (EGR2) Correlate with Severity of Human Myelinopathies

Human molecular genetics, 1999-07, Vol.8 (7), p.1245-1251

1999

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Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype

Neurology, 1999-06, Vol.52 (9), p.1827-1827

1999

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Expression of Dp260 in muscle tethers the actin cytoskeleton to the dystrophin–glycoprotein complex and partially prevents dystrophy

Human molecular genetics, 2002-05, Vol.11 (9), p.1095-1105

2002

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Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth disease

Muscle & nerve, 2000-02, Vol.23 (2), p.182-188

2000

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HEREDITARY PERIPHERAL NEUROPATHIES: Clinical Forms, Genetics, and Molecular Mechanisms

Annual review of medicine, 1999-01, Vol.50 (1), p.263-275

1999

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Comparing the viscoelastic properties of gelatin and different concentrations of kappa-carrageenan mixtures for additive manufacturing applications

Journal of food engineering, 2019-04, Vol.246, p.58-66

2019

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Clinical Phenotypes of Different MPZ (P 0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination

Neuron (Cambridge, Mass.), 1996-09, Vol.17 (3), p.451-460

1996

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Congenital hypomyelinating neuropathy: two patients with long-term follow-up

Pediatric neurology, 1999-03, Vol.20 (3), p.226-232

1999

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Supplemental security income and social security disability insurance coverage among long-term childhood cancer survivors

JNCI : Journal of the National Cancer Institute, 2015-06, Vol.107 (6), p.djv057-djv057

2015

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Molecular Mechanisms for CMT1A Duplication and HNPP Deletion

Annals of the New York Academy of Sciences, 1999-10, Vol.883 (1), p.22-35

1999

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Molecular Mechanisms for CMT1A Duplication and HNPP Deletion

Annals of the New York Academy of Sciences, 1999-10, Vol.883 (1), p.22

1999

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Caregiver Intention To Restart Vaccinations After Childhood Cancer Treatment

Cancer epidemiology, biomarkers & prevention, 2019-03, Vol.28 (3), p.622-623

2019

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The Role of Geographic Factors in Human Papillomavirus (HPV) Vaccine Uptake Among Adolescent Girls in the United States

Cancer epidemiology, biomarkers & prevention, 2015-04, Vol.24 (4), p.758-758

2015

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Quality of Life and Comorbidities Impact Education and Employment for Survivors of Adolescent and Young Adult Cancers

Cancer epidemiology, biomarkers & prevention, 2014-03, Vol.23 (3), p.568-568

2014

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Comparison of single-strand conformation polymorphism and heteroduplex analysis for detection of mutations in Charcot-Marie-Tooth type 1 disease and related peripheral neuropathies

European journal of human genetics : EJHG, 1996, Vol.4 (6), p.329-333

1996

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Plasminogen Activator and Plasminogen Activator Inhibitor Gene Expression in Human Saphenous Vein Organ Culture

Experimental and molecular pathology, 2001-04, Vol.70 (2), p.146-153

2001

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Settling the myelin protein zero question in CMT1B

Nature genetics, 1995-10, Vol.11 (2), p.119-120

1995

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Facilitating condom use with clients during commercial sex in Nevada's legal brothels

American journal of public health (1971), 1998-04, Vol.88 (4), p.643-646

1998

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Molecular mechanisms for Charcot-Marie-Tooth disease and related demyelinating peripheral neuropathies

Cold Spring Harbor Symposia on Quantitative Biology, 1996, Vol.61, p.659

1996

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Vasodilative and anti-adrenergic effects of adenosine in diabetic rat hearts

Canadian journal of physiology and pharmacology, 1992-01, Vol.70 (1), p.13-19

1992

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Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease

Human mutation, 1996, Vol.7 (1), p.36-45

1996

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Multiple de novo MPZ (P0) point mutations in a sporadic Dejerine-Sottas case

Human mutation, 1997, Vol.10 (1), p.21-24

1997

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Absence of PMP22 coding region mutations in CMT1A duplication patients: Further evidence supporting gene dosage as a mechanism for charcot-marie-tooth disease type 1A

Human mutation, 1996, Vol.8 (4), p.362-365

1996

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Rural transformations and rural policies in the US and UK

1st edition., 2012

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Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

Functional Consequences of Mutations in the Early Growth Response 2 Gene (EGR2) Correlate with Severity of Human Myelinopathies

Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype

Expression of Dp260 in muscle tethers the actin cytoskeleton to the dystrophin–glycoprotein complex and partially prevents dystrophy

Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth disease

HEREDITARY PERIPHERAL NEUROPATHIES: Clinical Forms, Genetics, and Molecular Mechanisms

Comparing the viscoelastic properties of gelatin and different concentrations of kappa-carrageenan mixtures for additive manufacturing applications

Clinical Phenotypes of Different MPZ (P 0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination

Congenital hypomyelinating neuropathy: two patients with long-term follow-up

Supplemental security income and social security disability insurance coverage among long-term childhood cancer survivors

Molecular Mechanisms for CMT1A Duplication and HNPP Deletion

Molecular Mechanisms for CMT1A Duplication and HNPP Deletion

Caregiver Intention To Restart Vaccinations After Childhood Cancer Treatment

The Role of Geographic Factors in Human Papillomavirus (HPV) Vaccine Uptake Among Adolescent Girls in the United States

Quality of Life and Comorbidities Impact Education and Employment for Survivors of Adolescent and Young Adult Cancers

Comparison of single-strand conformation polymorphism and heteroduplex analysis for detection of mutations in Charcot-Marie-Tooth type 1 disease and related peripheral neuropathies

Plasminogen Activator and Plasminogen Activator Inhibitor Gene Expression in Human Saphenous Vein Organ Culture

Settling the myelin protein zero question in CMT1B

Facilitating condom use with clients during commercial sex in Nevada's legal brothels

Molecular mechanisms for Charcot-Marie-Tooth disease and related demyelinating peripheral neuropathies

Vasodilative and anti-adrenergic effects of adenosine in diabetic rat hearts

Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease

Multiple de novo MPZ (P0) point mutations in a sporadic Dejerine-Sottas case

Absence of PMP22 coding region mutations in CMT1A duplication patients: Further evidence supporting gene dosage as a mechanism for charcot-marie-tooth disease type 1A

Rural transformations and rural policies in the US and UK

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