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Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

Experimental neurology, 1989-11, Vol.106 (2), p.204-206

1989

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Increased oxidative stress and decreased activities of Ca2+/Mg2+-ATPase and Na+/K+-ATPase in the red blood cells of the hibernating black bear

Life sciences (1973), 2002-05, Vol.71 (2), p.153-161

2002

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RNAs That Interact with the Fragile X Syndrome RNA Binding Protein FMRP

Biochemical and biophysical research communications, 2000-09, Vol.275 (3), p.973-980

2000

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Analysis by high-performance liquid chromatography of hyaluronic acid and chondrotin sulfates

Analytical biochemistry, 1986-08, Vol.157 (1), p.93-99

1986

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Alteration in amino-glycerophospholipids levels in the plasma of children with autism: A potential biochemical diagnostic marker

Life sciences (1973), 2004-02, Vol.74 (13), p.1635-1643

2004

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Long-term changes in calbindin D28K immunoreactivity in the rat hippocampus after cardiac arrest

Neuroscience letters, 2002-03, Vol.321 (1-2), p.90-94

2002

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Long-term changes in calbindin D 28K immunoreactivity in the rat hippocampus after cardiac arrest

Neuroscience letters, 2002-03, Vol.321 (1), p.90-94

2002

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Increased oxidative stress and decreased activities of Ca 2+/Mg 2+-ATPase and Na +/K +-ATPase in the red blood cells of the hibernating black bear

Life sciences (1973), 2002, Vol.71 (2), p.153-161

2002

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Response to nutritional and growth hormone treatment in progeria

Metabolism, clinical and experimental, 1997-08, Vol.46 (8), p.851-856

1997

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Late Infantile Neuronal Ceroid Lipofuscinosis Is Due to Splicing Mutations in the CLN2 Gene

Molecular genetics and metabolism, 1999-06, Vol.67 (2), p.162-168

1999

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Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome

Experimental neurology, 1990-06, Vol.108 (3), p.247-250

1990

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Complications of mitral valve prolapse: Disproportionate occurrence in men and older patients

The American journal of medicine, 1986, Vol.81 (5), p.751-758

1986

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Bipolar spectrum disorder and fragile X syndrome: A family study

Biological psychiatry (1969), 1993-02, Vol.33 (3), p.213-216

1993

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Chapter 8 - Delayed Development of the Claustrum in Autism

The Claustrum, 2014, p.225-235

2014

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A profile of cognitive deficit in females from fragile x families

Neuropsychologia, 1986, Vol.24 (3), p.405-409

1986

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Localization of a human gene homologous to the PrP gene on the p ARM of chromosome 20 and detection of PrP-related antigens in normal human brain

Biochemical and biophysical research communications, 1986-10, Vol.140 (2), p.758-765

1986

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A PvuII RFLP detected in the human prion protein (PrP) gene

Nucleic acids research, 1987-04, Vol.15 (7), p.3191-3191

1987

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Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28

Genomics (San Diego, Calif.), 1992-04, Vol.12 (4), p.710-714

1992

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PFGE of human DNA: 5-azacytidine improves restriction

Nucleic acids research, 1987-04, Vol.15 (7), p.3183-3183

1987

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A high frequency NcoI RFLP detected in the Aizheimer amyloid peptide gene

Nucleic acids research, 1988-02, Vol.16 (4), p.1647-1647

1988

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Urinary hyaluronic acid elevation in Hutchinson-Gilford progeria syndrome

Mechanisms of ageing and development, 1986-06, Vol.35 (1), p.39-46

1986

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IN-SITU HYBRIDISATION OF THE β-AMYLOID PROTEIN PROBE TO CHROMOSOME 9 IN PATIENTS WITH FAMILIAL ALZHEIMER'S DISEASE

The Lancet (British edition), 1987-11, Vol.330 (8568), p.1155-1156

1987

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Fine mapping of an Alzheimer Disease-associated gene encoding beta-amyloid protein

Biochemical and biophysical research communications, 1988-02, Vol.151 (1), p.1-8

1988

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Isolation and regional localization by [formula omitted][formula omitted] hybridization of a unique gene segment to chromosome 21

Biochemical and biophysical research communications, 1984, Vol.121 (1), p.380-385

1984

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Complications of mitral valve prolapse

The American journal of medicine, 1986-11, Vol.81 (5), p.751-758

1986

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Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

Increased oxidative stress and decreased activities of Ca2+/Mg2+-ATPase and Na+/K+-ATPase in the red blood cells of the hibernating black bear

RNAs That Interact with the Fragile X Syndrome RNA Binding Protein FMRP

Analysis by high-performance liquid chromatography of hyaluronic acid and chondrotin sulfates

Alteration in amino-glycerophospholipids levels in the plasma of children with autism: A potential biochemical diagnostic marker

Long-term changes in calbindin D28K immunoreactivity in the rat hippocampus after cardiac arrest

Long-term changes in calbindin D 28K immunoreactivity in the rat hippocampus after cardiac arrest

Increased oxidative stress and decreased activities of Ca 2+/Mg 2+-ATPase and Na +/K +-ATPase in the red blood cells of the hibernating black bear

Response to nutritional and growth hormone treatment in progeria

Late Infantile Neuronal Ceroid Lipofuscinosis Is Due to Splicing Mutations in the CLN2 Gene

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome

Complications of mitral valve prolapse: Disproportionate occurrence in men and older patients

Bipolar spectrum disorder and fragile X syndrome: A family study

Chapter 8 - Delayed Development of the Claustrum in Autism

A profile of cognitive deficit in females from fragile x families

Localization of a human gene homologous to the PrP gene on the p ARM of chromosome 20 and detection of PrP-related antigens in normal human brain

A PvuII RFLP detected in the human prion protein (PrP) gene

Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28

PFGE of human DNA: 5-azacytidine improves restriction

A high frequency NcoI RFLP detected in the Aizheimer amyloid peptide gene

Urinary hyaluronic acid elevation in Hutchinson-Gilford progeria syndrome

IN-SITU HYBRIDISATION OF THE β-AMYLOID PROTEIN PROBE TO CHROMOSOME 9 IN PATIENTS WITH FAMILIAL ALZHEIMER'S DISEASE

Fine mapping of an Alzheimer Disease-associated gene encoding beta-amyloid protein

Isolation and regional localization by [formula omitted][formula omitted] hybridization of a unique gene segment to chromosome 21

Complications of mitral valve prolapse

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