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ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

Nature genetics, 2000-02, Vol.24 (2), p.120-125

2000

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Pregnancy of a patient with multiple Acyl-CoA dehydrogenation deficiency (MADD)

Molecular genetics and metabolism, 2012-08, Vol.106 (4), p.491-494

2012

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The Hegemon's Post-Soviet Hangover

Revolutionary Russia, 2019-07, Vol.32 (2), p.296-303

Melancon, Michael S

2019

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Abstract No. 502 Electrospun Bioresorbable Polymer Blends as Vascular Grafts

Journal of vascular and interventional radiology, 2024-03, Vol.35 (3), p.S180-S181

2024

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Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion

Annals of neurology, 1997-05, Vol.41 (5), p.675-682

1997

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Abstract No. 387 Fabrication of a Radiopaque, Drug-Eluting Resorbable Polymer for Medical Device Development

Journal of vascular and interventional radiology, 2024-03, Vol.35 (3), p.S172-S172

2024

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Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment

Journal of Medical Genetics, 2006-01, Vol.43 (1), p.1-11

2006

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Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11

American journal of human genetics, 1999-03, Vol.64 (3), p.768-775

1999

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Selective deep catalytic cracking process (SDCC) of petroleum feedstocks for the production of light olefins. I. The catlever effect obtained with a two reaction-zones system on the conversion of n-hexane

Catalysis letters, 2001-01, Vol.73 (2-4), p.181-186

2001

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Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay (ARSACS): High-Resolution Physical and Transcript Map of the Candidate Region in Chromosome Region 13q11

Genomics (San Diego, Calif.), 1999-12, Vol.62 (2), p.156-164

1999

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GAA Instability in Friedreich's Ataxia Shares a Common, DNA-Directed and Intraallelic Mechanism with Other Trinucleotide Diseases

Molecular cell, 1998-03, Vol.1 (4), p.583-593

1998

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The Hegemon's Post-Soviet Hangover: Iu. V. Aksiutin. Posleoktiabr'skoe pokhmel'e gegemona: Rabochii klass i politicheskie partii Rossii v pervyi god sovetskoi vlasti (noiabr' 1917 - konets 1918 gg.). Moscow: MGOU, 2013.410 pages. ISBN: 978-5-7017-2174-4

Revolutionary Russia, 2019-07, Vol.32 (2), p.296-303

Melancon, Michael S.

2019

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Neurologic Crises in Hereditary Tyrosinemia

The New England journal of medicine, 1990-02, Vol.322 (7), p.432-437

1990

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Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype

Journal of medical genetics, 2011-09, Vol.48 (9), p.602-605

2011

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An unusual splicing mutation in the HEXB gene is associated with dramatically different phenotypes in patients from different racial backgrounds

The Journal of clinical investigation, 1992-08, Vol.90 (2), p.306-314

1992

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Prenatal diagnosis of smith-lemli-opitz syndrome is possible by measurement of 7-dehydrocholesterol in amniotic fluid

Prenatal diagnosis, 1995-09, Vol.15 (9), p.855-858

1995

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Black Female Sexualities

1, 2015

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Methods for Multilevel Analysis and Visualisation of Geographical Networks

2013, 2013

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Prenatal diagnosis of fetal anomalies during the second trimester of pregnancy: Their characterization and delineation of defects in pregnancies at risk

Prenatal diagnosis, 1991-08, Vol.11 (8), p.629-635

1991

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Fluorometric assay of neuraminidase with a sodium (4-methylumbelliferyl-α- d- N-acetylneuraminate) substrate

Analytical biochemistry, 1979-04, Vol.94 (2), p.287-296

1979

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Clinical spectrum of infantile free sialic acid storage disease

American journal of medical genetics, 1999-02, Vol.82 (5), p.385-391

1999

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Genetic homogeneity at the Friedreich ataxia locus on chromosome 9

American journal of human genetics, 1989-04, Vol.44 (4), p.518-521

1989

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Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): Confirmation of close linkage to D5S39 in French Canadian families

Genomics (San Diego, Calif.), 1992-09, Vol.14 (1), p.188-190

1992

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Fast Stress and Rest Acquisitions for Technetium-99m-Sestamibi Separate-Day SPECT

The Journal of nuclear medicine (1978), 1995-04, Vol.36 (4), p.569-574

1995

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Screening for Pompe Disease in Specific At-Risk Populations with Sleep-Disordered Breathing

Journal of neuromuscular diseases, 2015, Vol.2 (s1), p.S44-S44

2015

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ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

Pregnancy of a patient with multiple Acyl-CoA dehydrogenation deficiency (MADD)

The Hegemon's Post-Soviet Hangover

Abstract No. 502 Electrospun Bioresorbable Polymer Blends as Vascular Grafts

Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion

Abstract No. 387 Fabrication of a Radiopaque, Drug-Eluting Resorbable Polymer for Medical Device Development

Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment

Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11

Selective deep catalytic cracking process (SDCC) of petroleum feedstocks for the production of light olefins. I. The catlever effect obtained with a two reaction-zones system on the conversion of n-hexane

Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay (ARSACS): High-Resolution Physical and Transcript Map of the Candidate Region in Chromosome Region 13q11

GAA Instability in Friedreich's Ataxia Shares a Common, DNA-Directed and Intraallelic Mechanism with Other Trinucleotide Diseases

The Hegemon's Post-Soviet Hangover: Iu. V. Aksiutin. Posleoktiabr'skoe pokhmel'e gegemona: Rabochii klass i politicheskie partii Rossii v pervyi god sovetskoi vlasti (noiabr' 1917 - konets 1918 gg.). Moscow: MGOU, 2013.410 pages. ISBN: 978-5-7017-2174-4

Neurologic Crises in Hereditary Tyrosinemia

Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype

An unusual splicing mutation in the HEXB gene is associated with dramatically different phenotypes in patients from different racial backgrounds

Prenatal diagnosis of smith-lemli-opitz syndrome is possible by measurement of 7-dehydrocholesterol in amniotic fluid

Black Female Sexualities

Methods for Multilevel Analysis and Visualisation of Geographical Networks

Prenatal diagnosis of fetal anomalies during the second trimester of pregnancy: Their characterization and delineation of defects in pregnancies at risk

Fluorometric assay of neuraminidase with a sodium (4-methylumbelliferyl-α- d- N-acetylneuraminate) substrate

Clinical spectrum of infantile free sialic acid storage disease

Genetic homogeneity at the Friedreich ataxia locus on chromosome 9

Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): Confirmation of close linkage to D5S39 in French Canadian families

Fast Stress and Rest Acquisitions for Technetium-99m-Sestamibi Separate-Day SPECT

Screening for Pompe Disease in Specific At-Risk Populations with Sleep-Disordered Breathing

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