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Global maps of non-traumatic spinal cord injury epidemiology: towards a living data repository

Spinal cord, 2014-02, Vol.52 (2), p.97-109

2014

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Outcomes following stoma formation in patients with spinal cord injury

Colorectal disease, 2019-12, Vol.21 (12), p.1415-1420

2019

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Aggregation behavior of amphiphilic poly(2-alkyl-2-oxazoline) diblock copolymers in aqueous solution studied by fluorescence correlation spectroscopy

Colloid and polymer science, 2004-06, Vol.282 (8), p.833-843

2004

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The Emerging Tree of West Eurasian mtDNAs: A Synthesis of Control-Region Sequences and RFLPs

American journal of human genetics, 1999, Vol.64 (1), p.232-249

1999

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International Spinal Cord Injury Urinary Tract Infection Basic Data Set

Spinal cord, 2013-09, Vol.51 (9), p.700-704

2013

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Effect of Polymer Architecture of Amphiphilic Poly(2-oxazoline) Copolymers on the Aggregation and Aggregate Structure

Macromolecular chemistry and physics, 2007-07, Vol.208 (13), p.1402-1408

2007

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Y chromosome sequence variation and the history of human populations

Nature genetics, 2000-11, Vol.26 (3), p.358-361

2000

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Micellar Structures of Hydrophilic/Lipophilic and Hydrophilic/Fluorophilic Poly(2‐oxazoline) Diblock Copolymers in Water

Macromolecular chemistry and physics, 2008-11, Vol.209 (21), p.2248-2258

2008

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Short-term peripheral nerve stimulation ameliorates axonal dysfunction after spinal cord injury

Journal of neurophysiology, 2015-05, Vol.113 (9), p.3209-3218

2015

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Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins

Science (American Association for the Advancement of Science), 1996-03, Vol.271 (5254), p.1380-1387

1996

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Jewish and Middle Eastern Non-Jewish Populations Share a Common Pool of Y-Chromosome Biallelic Haplotypes

Proceedings of the National Academy of Sciences - PNAS, 2000-06, Vol.97 (12), p.6769-6774

2000

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mtDNA Analysis Reveals a Major Late Paleolithic Population Expansion from Southwestern to Northeastern Europe

American journal of human genetics, 1998-05, Vol.62 (5), p.1137-1152

1998

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Role of the tracer in characterizing the aggregation behavior of aqueous block copolymer solutions using fluorescence correlation spectroscopy

Colloid and polymer science, 2007-02, Vol.285 (5), p.491-497

2007

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Aggregation behavior of amphiphilic poly(2-alkyl-2-oxazoline) diblock copolymers in aqueous solution studied by fluorescence correlation spectroscopy

Colloid and polymer science, 2004-10, Vol.282 (12), p.1425-1425

2004

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Maternal and Paternal Lineages of the Samaritan Isolate: Mutation Rates and Time to Most Recent Common Male Ancestor

Annals of human genetics, 2003-03, Vol.67 (2), p.153-164

2003

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Global maps of non-traumatic spinal cord injury epidemiology: towards a living data repository

Spinal cord, 2014-05, Vol.52 (5), p.417-417

2014

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O-077: Failure in osteoporosis management after hip fracture

European geriatric medicine, 2015-09, Vol.6, p.S27-S27

2015

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Worldwide Genetic Analysis of the CFTR Region

American journal of human genetics, 2001-01, Vol.68 (1), p.103-117

2001

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The Habbanite Isolate

Human heredity, 2008-08, Vol.21 (5), p.478-492

2008

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Usher syndrome in the Samaritans: Strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders

American journal of physical anthropology, 1997-10, Vol.104 (2), p.193-200

1997

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Predictive testing for Wilson's disease using tightly linked and flanking DNA markers

Neurology, 1991-07, Vol.41 (7), p.992-992

1991

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Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3

American journal of human genetics, 1996-06, Vol.58 (6), p.1254-1259

1996

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Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

Human molecular genetics, 1995-09, Vol.4 (9), p.1637-1642

1995

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The Habbanite Isolate. III

Human heredity, 2008-08, Vol.22 (5-6), p.430-444

2008

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Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse Origins

American journal of human genetics, 1997-10, Vol.61 (4), p.813-821

1997

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Global maps of non-traumatic spinal cord injury epidemiology: towards a living data repository

Outcomes following stoma formation in patients with spinal cord injury

Aggregation behavior of amphiphilic poly(2-alkyl-2-oxazoline) diblock copolymers in aqueous solution studied by fluorescence correlation spectroscopy

The Emerging Tree of West Eurasian mtDNAs: A Synthesis of Control-Region Sequences and RFLPs

International Spinal Cord Injury Urinary Tract Infection Basic Data Set

Effect of Polymer Architecture of Amphiphilic Poly(2-oxazoline) Copolymers on the Aggregation and Aggregate Structure

Y chromosome sequence variation and the history of human populations

Micellar Structures of Hydrophilic/Lipophilic and Hydrophilic/Fluorophilic Poly(2‐oxazoline) Diblock Copolymers in Water

Short-term peripheral nerve stimulation ameliorates axonal dysfunction after spinal cord injury

Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins

Jewish and Middle Eastern Non-Jewish Populations Share a Common Pool of Y-Chromosome Biallelic Haplotypes

mtDNA Analysis Reveals a Major Late Paleolithic Population Expansion from Southwestern to Northeastern Europe

Role of the tracer in characterizing the aggregation behavior of aqueous block copolymer solutions using fluorescence correlation spectroscopy

Aggregation behavior of amphiphilic poly(2-alkyl-2-oxazoline) diblock copolymers in aqueous solution studied by fluorescence correlation spectroscopy

Maternal and Paternal Lineages of the Samaritan Isolate: Mutation Rates and Time to Most Recent Common Male Ancestor

Global maps of non-traumatic spinal cord injury epidemiology: towards a living data repository

O-077: Failure in osteoporosis management after hip fracture

Worldwide Genetic Analysis of the CFTR Region

The Habbanite Isolate

Usher syndrome in the Samaritans: Strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders

Predictive testing for Wilson's disease using tightly linked and flanking DNA markers

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

The Habbanite Isolate. III

Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse Origins

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