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Mutation detection in the ABCC6 gene and genotype–phenotype analysis in a large international case series affected by pseudoxanthoma elasticum

Journal of medical genetics, 2007-10, Vol.44 (10), p.621-628

2007

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Myoblast Transfer in the Treatment of Duchenne's Muscular Dystrophy

The New England journal of medicine, 1995-09, Vol.333 (13), p.832-838

1995

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Effect of Depth and Duration of Cooling on Death or Disability at Age 18 Months Among Neonates With Hypoxic-Ischemic Encephalopathy: A Randomized Clinical Trial

JAMA : the journal of the American Medical Association, 2017-07, Vol.318 (1), p.57

2017

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The Survival Motor Neuron Protein in Spinal Muscular Atrophy

Human molecular genetics, 1997-08, Vol.6 (8), p.1205-1214

1997

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Intragenic telSMN Mutations: Frequency, Distribution, Evidence of a Founder Effect, and Modification of the Spinal Muscular Atrophy Phenotype by cenSMN Copy Number

American journal of human genetics, 1998-12, Vol.63 (6), p.1712-1723

1998

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Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number

American journal of human genetics, 1997-06, Vol.60 (6), p.1411-1422

1997

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Repeated degradation and progradation of a submarine slope over geological timescales

Journal of sedimentary research, 2021-01, Vol.91 (1), p.116-145

2021

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Epidemic Adolescent Binge Drinking at Lollapalooza, A Music Festival in Chicago

Pediatric emergency care, 2019-06, Vol.35 (6), p.391-396

2019

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An 11 Base Pair Duplication in Exon 6 of the SMN Gene Produces a Type I Spinal Muscular Atrophy (SMA) Phenotype: Further Evidence For SMN as the Primary SMA-Determining Gene

Human molecular genetics, 1996-11, Vol.5 (11), p.1727-1732

1996

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Management of under-16-year olds in UK genitourinary medicine clinics: British Co-operative Clinical Group

International journal of STD & AIDS, 2008-09, Vol.19 (9), p.625-628

2008

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THE INCIDENCE OF THE GENE FOR THERMOLABILE METHYLENE TETRAHYDROFOLATE REDUCTASE IN AFRICAN AMERICANS

Thrombosis research, 1996-07, Vol.83 (2), p.195-198

1996

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Central Nervous System Herpes Simplex Virus Infection in Afebrile Children With Seizures

Journal of child neurology, 2012-04, Vol.27 (4), p.445-450

2012

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The relationship between self-esteem and language disordered children

Child language teaching and therapy, 1999-10, Vol.15 (3), p.219-232

McAndrew, E.

1999

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Diagnosis of spinal muscular atrophy in an SMN non-deletion patient using a quantitative PCR screen and mutation analysis

Journal of medical genetics, 1998-08, Vol.35 (8), p.674-676

1998

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Novel receptor protein tyrosine phosphatase (RPTPρ) and acidic fibroblast growth factor (FGF-1) transcripts delineate a rostrocaudal boundary in the granule cell layer of the murine cerebellar cortex

Journal of comparative neurology (1911), 1998-02, Vol.391 (4), p.444-455

1998

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Collaboration between civilian and military healthcare professionals: a better way for planning, preparing, and responding to all hazard domestic events

Prehospital and disaster medicine, 2010-10, Vol.25 (5), p.399-412

2010

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Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7

Neurogenetics, 1997-11, Vol.1 (2), p.141-147

1997

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Differential diagnosis of hereditary hemochromatosis from other liver disorders by genetic analysis: gene mutation analysis of patients previously diagnosed with hemochromatosis by liver biopsy

Archives of pathology & laboratory medicine (1976), 1998-07, Vol.122 (7), p.633

1998

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Identification and characterization of RPTP ρ, a novel RPTP μ/ κ-like receptor protein tyrosine phosphatase whose expression is restricted to the central nervous system

Brain research. Molecular brain research., 1998-05, Vol.56 (1), p.9-21

1998

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Amiloride-sensitive sodium-hydrogen exchange in osmotically shrunken rabbit red blood cells

American Journal of Physiology: Cell Physiology, 1986-07, Vol.251 (1), p.C32-C40

1986

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A hazard with the Abbott Provider 5500

Anaesthesia, 1995-09, Vol.50 (9), p.829-829

McAndrew, P.E.

1995

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Tissue Oxygenation Changes After Transfusion and Outcomes in Preterm Infants: A Secondary Near-Infrared Spectroscopy Study of the Transfusion of Prematures Randomized Clinical Trial (TOP NIRS)

JAMA network open, 2023-09, Vol.6 (9), p.e2334889-e2334889

2023

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Murine TH response to influenza virus: recognition of hemagglutinin, neuraminidase, matrix, and nucleoproteins

The Journal of immunology (1950), 1985-03, Vol.134 (3), p.1994-1998

1985

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Anti-Thy-1 plus complement-treated, cultured bone marrow cells resemble fetal thymocytes in killer cell function and marker expression

The Journal of immunology (1950), 1986-09, Vol.137 (6), p.1757-1763

1986

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The relationship between self-esteem and language disordered children

Child language teaching and therapy, 1999-10, Vol.15 (3), p.219-232

McAndrew, Edel

1999

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Mutation detection in the ABCC6 gene and genotype–phenotype analysis in a large international case series affected by pseudoxanthoma elasticum

Myoblast Transfer in the Treatment of Duchenne's Muscular Dystrophy

Effect of Depth and Duration of Cooling on Death or Disability at Age 18 Months Among Neonates With Hypoxic-Ischemic Encephalopathy: A Randomized Clinical Trial

The Survival Motor Neuron Protein in Spinal Muscular Atrophy

Intragenic telSMN Mutations: Frequency, Distribution, Evidence of a Founder Effect, and Modification of the Spinal Muscular Atrophy Phenotype by cenSMN Copy Number

Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number

Repeated degradation and progradation of a submarine slope over geological timescales

Epidemic Adolescent Binge Drinking at Lollapalooza, A Music Festival in Chicago

An 11 Base Pair Duplication in Exon 6 of the SMN Gene Produces a Type I Spinal Muscular Atrophy (SMA) Phenotype: Further Evidence For SMN as the Primary SMA-Determining Gene

Management of under-16-year olds in UK genitourinary medicine clinics: British Co-operative Clinical Group

THE INCIDENCE OF THE GENE FOR THERMOLABILE METHYLENE TETRAHYDROFOLATE REDUCTASE IN AFRICAN AMERICANS

Central Nervous System Herpes Simplex Virus Infection in Afebrile Children With Seizures

The relationship between self-esteem and language disordered children

Diagnosis of spinal muscular atrophy in an SMN non-deletion patient using a quantitative PCR screen and mutation analysis

Novel receptor protein tyrosine phosphatase (RPTPρ) and acidic fibroblast growth factor (FGF-1) transcripts delineate a rostrocaudal boundary in the granule cell layer of the murine cerebellar cortex

Collaboration between civilian and military healthcare professionals: a better way for planning, preparing, and responding to all hazard domestic events

Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7

Differential diagnosis of hereditary hemochromatosis from other liver disorders by genetic analysis: gene mutation analysis of patients previously diagnosed with hemochromatosis by liver biopsy

Identification and characterization of RPTP ρ, a novel RPTP μ/ κ-like receptor protein tyrosine phosphatase whose expression is restricted to the central nervous system

Amiloride-sensitive sodium-hydrogen exchange in osmotically shrunken rabbit red blood cells

A hazard with the Abbott Provider 5500

Tissue Oxygenation Changes After Transfusion and Outcomes in Preterm Infants: A Secondary Near-Infrared Spectroscopy Study of the Transfusion of Prematures Randomized Clinical Trial (TOP NIRS)

Murine TH response to influenza virus: recognition of hemagglutinin, neuraminidase, matrix, and nucleoproteins

Anti-Thy-1 plus complement-treated, cultured bone marrow cells resemble fetal thymocytes in killer cell function and marker expression

The relationship between self-esteem and language disordered children

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