Scientific Commons: Rob Curtain

Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population (2008)

Lotti Tajouri, Micky Ovcaric, Rob Curtain, Matthew P. Johnson, R. Griffiths, Peter Csurhes, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Investigation of the NOTCH3 and TNFSF7 Genes on C19p13 as Candidates for Migraine (2008)

Smith, Robert Anthony, Curtain, Rob, Ovcaric, Micky, Tajouri, Lotfi, MacMillan, John, Griffiths, Lyn

To investigate the migraine locus around the C19p13 region through analysis of the NOTCH3 gene (C19p13.2- p13.1), previously shown to be a gene involved in CADASIL and the TNFSF7 gene (C19p13),...

Investigation of the NOTCH3 and TNFSF7 Genes on C19p13 as Candidates for Migraine (2008)

Smith, Robert Anthony, Curtain, Rob, Ovcaric, Micky, Tajouri, Lotfi, MacMillan, John, Griffiths, Lyn

To investigate the migraine locus around the C19p13 region through analysis of the NOTCH3 gene (C19p13.2- p13.1), previously shown to be a gene involved in CADASIL and the TNFSF7 gene (C19p13),...

Investigation of the NOTCH3 and TNFSF7 Genes on C19p13 as Candidates for Migraine (2008)

Smith, Robert Anthony, Curtain, Rob, Ovcaric, Micky, Tajouri, Lotfi, MacMillan, John, Griffiths, Lyn

To investigate the migraine locus around the C19p13 region through analysis of the NOTCH3 gene (C19p13.2- p13.1), previously shown to be a gene involved in CADASIL and the TNFSF7 gene (C19p13),...

Association analysis of chromosome 1 migraine candidate genes (2007)

Fernandez, Francesca, Curtain, Rob, Colson, Natalie Jane, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine with aura (MA) is a subtype of typical migraine. Migraine with aura (MA) also encompasses a rare severe subtype Familial Hemiplegic Migraine (FHM) with several known genetic loci....

Association analysis of chromosome 1 migraine candidate genes (2007)

Fernandez, Francesca, Curtain, Rob, Colson, Natalie Jane, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine with aura (MA) is a subtype of typical migraine. Migraine with aura (MA) also encompasses a rare severe subtype Familial Hemiplegic Migraine (FHM) with several known genetic loci....

Association analysis of chromosome 1 migraine candidate genes (2007)

Fernandez, Francesca, Curtain, Rob, Colson, Natalie Jane, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine with aura (MA) is a subtype of typical migraine. Migraine with aura (MA) also encompasses a rare severe subtype Familial Hemiplegic Migraine (FHM) with several known genetic loci....

Genetic Investigation of Methylenetetrahydrofolate Reductase (MTHFR) and Catechol-O-Methyl Transferase (COMT) in Multiple Sclerosis (2006)

Tajouri, Lotti, Martin, Virginie, Gasparini, Claudia, Ovcaric, Micky, Curtain, Rob, Lea, Rod A., ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Genetic Investigation of Methylenetetrahydrofolate Reductase (MTHFR) and Catechol-O-Methyl Transferase (COMT) in Multiple Sclerosis (2006)

Tajouri, Lotti, Martin, Virginie, Gasparini, Claudia, Ovcaric, Micky, Curtain, Rob, Lea, Rod A., ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Minor Head Trauma Induced Sporadic Hemiplegic Migraine (SHM) Coma (2006)

Curtain, Rob, Smith, Robert Anthony, Ovcaric, Micky, Griffiths, Lyn

Familial hemiplegic migraine is a severe, rare subtype of migraine. Gene mutations on chromosome 19 have been identified in the calcium channel, voltage-dependent, P/Q type, alpha-1A subunit gene...

Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol-O-methyl transferase (COMT) in multiple sclerosis (2006)

Tajouri, Lotfi, Martin, Virginie, Gasparini, Claudia Francesca, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree (2006)

Curtain, Rob, Tajouri, Lotfi, Lea, Rodney Arthur, MacMillan, John, Griffiths, Lyn

The aim of this study was to investigate through direct sequencing the insulin receptor (INSR) gene in DNA samples from a migraine affected family previously showing linkage to chromosome 19p13 in an...

Minor Head Trauma Induced Sporadic Hemiplegic Migraine (SHM) Coma (2006)

Curtain, Rob, Smith, Robert Anthony, Ovcaric, Micky, Griffiths, Lyn

Yes

Genetic investigation of methylenetetrahydroxyfolate reductase (MTHFR) and catechol-o-methyl transferase (COMT) in multiple sclerosis. (2006)

Tajouri, Lotfi, Martin, Virginie, Gasparini, Claudia Francesca, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, ...

Yes

No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree (2006)

Curtain, Rob, Tajouri, Lotfi, Lea, Rodney Arthur, MacMillan, John, Griffiths, Lyn

Yes

Association of the Vitamin D Receptor Gene with Multiple Sclerosis (2006)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Johnson, Matthew Peter, Csurhes, P., ...

No

Association of the Vitamin D Receptor Gene with Multiple Sclerosis (2006)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Johnson, Matthew Peter, Csurhes, P., ...

No

Minor Head Trauma Induced Sporadic Hemiplegic Migraine (SHM) Coma (2006)

Curtain, Rob, Smith, Robert Anthony, Ovcaric, Micky, Griffiths, Lyn

Familial hemiplegic migraine is a severe, rare subtype of migraine. Gene mutations on chromosome 19 have been identified in the calcium channel, voltage-dependent, P/Q type, alpha-1A subunit gene...

Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol-O-methyl transferase (COMT) in multiple sclerosis (2006)

Tajouri, Lotfi, Martin, Virginie, Gasparini, Claudia Francesca, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree (2006)

Curtain, Rob, Tajouri, Lotfi, Lea, Rodney Arthur, MacMillan, John, Griffiths, Lyn

The aim of this study was to investigate through direct sequencing the insulin receptor (INSR) gene in DNA samples from a migraine affected family previously showing linkage to chromosome 19p13 in an...

Association of the Vitamin D Receptor Gene with Multiple Sclerosis (2006)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Johnson, Matthew Peter, Csurhes, P., ...

Genetic Investigation of Methylenetetrahydrofolate Reductase (MTHFR) and Catechol-O-Methyl Transferase (COMT) in Multiple Sclerosis (2006)

Tajouri, Lotti, Martin, Virginie, Gasparini, Claudia, Ovcaric, Micky, Curtain, Rob, Lea, Rod A., ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Genetic Investigation of Methylenetetrahydrofolate Reductase (MTHFR) and Catechol-O-Methyl Transferase (COMT) in Multiple Sclerosis (2006)

Tajouri, Lotti, Martin, Virginie, Gasparini, Claudia, Ovcaric, Micky, Curtain, Rob, Lea, Rod A., ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Minor Head Trauma Induced Sporadic Hemiplegic Migraine (SHM) Coma (2006)

Curtain, Rob, Smith, Robert Anthony, Ovcaric, Micky, Griffiths, Lyn

Familial hemiplegic migraine is a severe, rare subtype of migraine. Gene mutations on chromosome 19 have been identified in the calcium channel, voltage-dependent, P/Q type, alpha-1A subunit gene...

Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol-O-methyl transferase (COMT) in multiple sclerosis (2006)

Tajouri, Lotfi, Martin, Virginie, Gasparini, Claudia Francesca, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree (2006)

Curtain, Rob, Tajouri, Lotfi, Lea, Rodney Arthur, MacMillan, John, Griffiths, Lyn

The aim of this study was to investigate through direct sequencing the insulin receptor (INSR) gene in DNA samples from a migraine affected family previously showing linkage to chromosome 19p13 in an...

Association of the Vitamin D Receptor Gene with Multiple Sclerosis (2006)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Johnson, Matthew Peter, Csurhes, P., ...

Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population (2005)

Tajouri, Lotti, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew P., Griffiths, Lyn R., Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility. (2005)

Curtain, Rob, Sundholm, James Rodney, Lea, Rodney Arthur, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn, ...

Page numbers are not for citation purposes. Instead, this article has the unique article number of 32.

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine. (2005)

Lea, Rodney Arthur, Nyholt, D. R., Curtain, Rob, Ovcaric, Micky, Sciascia, Rachel, Bellis, Claire, ...

Yes

Variation in the vitamin D receptor gene is associated with multiple sclerosis in an Australian population. (2005)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew Peter, Griffiths, Lyn, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility. (2005)

Curtain, Rob, Sundholm, James Rodney, Lea, Rodney Arthur, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine is a polygenic multifactorial disease, possessing environmental and genetic causative factors with multiple involved genes. Mutations in various ion channel genes are responsible...

Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees (2005)

Curtain, Rob, Lea, Rodney Arthur, Tajouri, Lotfi, Haupt, Larisa, Ovcaric, Micky, MacMillan, J., ...

Yes

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine. (2005)

Lea, Rodney Arthur, Nyholt, D. R., Curtain, Rob, Ovcaric, Micky, Sciascia, Rachel, Bellis, Claire, ...

Migraine is a prevalent neurovascular disease with a significant genetic component. Linkage studies have so far identified migraine susceptibility loci on chromosomes 1, 4, 6, 11, 14, 19 and X. We...

Variation in the vitamin D receptor gene is associated with multiple sclerosis in an Australian population. (2005)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew Peter, Griffiths, Lyn, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility. (2005)

Curtain, Rob, Sundholm, James Rodney, Lea, Rodney Arthur, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine is a polygenic multifactorial disease, possessing environmental and genetic causative factors with multiple involved genes. Mutations in various ion channel genes are responsible...

Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees (2005)

Curtain, Rob, Lea, Rodney Arthur, Tajouri, Lotfi, Haupt, Larisa, Ovcaric, Micky, MacMillan, J., ...

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine. (2005)

Lea, Rodney Arthur, Nyholt, D. R., Curtain, Rob, Ovcaric, Micky, Sciascia, Rachel, Bellis, Claire, ...

Migraine is a prevalent neurovascular disease with a significant genetic component. Linkage studies have so far identified migraine susceptibility loci on chromosomes 1, 4, 6, 11, 14, 19 and X. We...

Variation in the vitamin D receptor gene is associated with multiple sclerosis in an Australian population. (2005)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew Peter, Griffiths, Lyn, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population (2005)

Tajouri, Lotti, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew P., Griffiths, Lyn R., Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population (2005)

Tajouri, Lotti, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew P., Griffiths, Lyn R., Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility. (2005)

Curtain, Rob, Sundholm, James Rodney, Lea, Rodney Arthur, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine is a polygenic multifactorial disease, possessing environmental and genetic causative factors with multiple involved genes. Mutations in various ion channel genes are responsible...

Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees (2005)

Curtain, Rob, Lea, Rodney Arthur, Tajouri, Lotfi, Haupt, Larisa, Ovcaric, Micky, MacMillan, J., ...

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine. (2005)

Lea, Rodney Arthur, Nyholt, D. R., Curtain, Rob, Ovcaric, Micky, Sciascia, Rachel, Bellis, Claire, ...

Migraine is a prevalent neurovascular disease with a significant genetic component. Linkage studies have so far identified migraine susceptibility loci on chromosomes 1, 4, 6, 11, 14, 19 and X. We...

Variation in the vitamin D receptor gene is associated with multiple sclerosis in an Australian population. (2005)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew Peter, Griffiths, Lyn, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Investigation of a Neuronal Nitric Oxide Synthase Gene (NOS1) Polymorphism in a Multiple Sclerosis Population (2004)

Tajouri, Lotti, Ferreira, Linda, Ovcaric, Micky, Curtain, Rob, Lea, Rod, Csurhes, Peter A., ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Investigation of a Neuronal Nitric Oxide Synthase Gene (NOS1) Polymorphism in a Multiple Sclerosis Population (2004)

Tajouri, Lotti, Ferreira, Linda, Ovcaric, Micky, Curtain, Rob, Lea, Rod, Csurhes, Peter A., ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine (2004)

Curtain, Rob, Lea, Rodney Arthur, Quinlan, Sharon, Bellis, Claire, Tajouri, Lotfi, Hughes, Roger Michael, ...

The Low-Density Lipoprotein Receptor (LDLR) gene is a cell surface receptor that plays an important role in cholesterol homeostasis. We investigated the (TA)n polymorphism in exon 18 of the LDLR gene...

Implication of Vascular and Hormonal Gene Variants in Migraine Susceptibility (2004)

Griffiths, Lyn, Lea, Rodney Arthur, Johnson, Matthew Peter, Colson, Natalie Jane, Curtain, Rob, Quinlan, Sharon, ...

No

Migraine Susceptibility: Role for Vascular and Hormonal Gene Variants (2004)

Griffiths, Lyn, Colson, Natalie Jane, Johnson, Matthew Peter, Curtain, Rob, Quinlan, Sharon, MacMillan, J, ...

No

Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine (2004)

Curtain, Rob, Lea, Rodney Arthur, Quinlan, Sharon, Bellis, Claire, Tajouri, Lotfi, Hughes, Roger Michael, ...

The Low-Density Lipoprotein Receptor (LDLR) gene is a cell surface receptor that plays an important role in cholesterol homeostasis. We investigated the (TA)n polymorphism in exon 18 of the LDLR gene...

Investigation of an unducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Martin, Virginie, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Ferreira, Linda Anne, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Implication of Vascular and Hormonal Gene Variants in Migraine Susceptibility (2004)

Griffiths, Lyn, Lea, Rodney Arthur, Johnson, Matthew Peter, Colson, Natalie Jane, Curtain, Rob, Quinlan, Sharon, ...

No

Migraine Susceptibility: Role for Vascular and Hormonal Gene Variants (2004)

Griffiths, Lyn, Colson, Natalie Jane, Johnson, Matthew Peter, Curtain, Rob, Quinlan, Sharon, MacMillan, J

No

Vascular and Hormonal Variants are Implicated in Migraine Susceptibility (2004)

Griffiths, Lyn, Lea, Rodney Arthur, Colson, Natalie Jane, Johnson, Matthew Peter, Curtain, Rob, Quinlan, Sharon, ...

No

Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine (2004)

Curtain, Rob, Lea, Rodney Arthur, Quinlan, Sharon, Bellis, Claire, Tajouri, Lotfi, Hughes, Roger Michael, ...

The Low-Density Lipoprotein Receptor (LDLR) gene is a cell surface receptor that plays an important role in cholesterol homeostasis. We investigated the (TA)n polymorphism in exon 18 of the LDLR gene...

Investigation of an unducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Martin, Virginie, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Ferreira, Linda Anne, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Implication of Vascular and Hormonal Gene Variants in Migraine Susceptibility (2004)

Griffiths, Lyn, Lea, Rodney Arthur, Johnson, Matthew Peter, Colson, Natalie Jane, Curtain, Rob, Quinlan, Sharon, ...

Migraine Susceptibility: Role for Vascular and Hormonal Gene Variants (2004)

Griffiths, Lyn, Colson, Natalie Jane, Johnson, Matthew Peter, Curtain, Rob, Quinlan, Sharon, MacMillan, J

Vascular and Hormonal Variants are Implicated in Migraine Susceptibility (2004)

Griffiths, Lyn, Lea, Rodney Arthur, Colson, Natalie Jane, Johnson, Matthew Peter, Curtain, Rob, Quinlan, Sharon, ...

Investigation of a Neuronal Nitric Oxide Synthase Gene (NOS1) Polymorphism in a Multiple Sclerosis Population (2004)

Tajouri, Lotti, Ferreira, Linda, Ovcaric, Micky, Curtain, Rob, Lea, Rod, Csurhes, Peter A., ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Investigation of a Neuronal Nitric Oxide Synthase Gene (NOS1) Polymorphism in a Multiple Sclerosis Population (2004)

Tajouri, Lotti, Ferreira, Linda, Ovcaric, Micky, Curtain, Rob, Lea, Rod, Csurhes, Peter A., ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine (2004)

Curtain, Rob, Lea, Rodney Arthur, Quinlan, Sharon, Bellis, Claire, Tajouri, Lotfi, Hughes, Roger Michael, ...

The Low-Density Lipoprotein Receptor (LDLR) gene is a cell surface receptor that plays an important role in cholesterol homeostasis. We investigated the (TA)n polymorphism in exon 18 of the LDLR gene...

Investigation of an unducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Martin, Virginie, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Ferreira, Linda Anne, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Implication of Vascular and Hormonal Gene Variants in Migraine Susceptibility (2004)

Griffiths, Lyn, Lea, Rodney Arthur, Johnson, Matthew Peter, Colson, Natalie Jane, Curtain, Rob, Quinlan, Sharon, ...

Migraine Susceptibility: Role for Vascular and Hormonal Gene Variants (2004)

Griffiths, Lyn, Colson, Natalie Jane, Johnson, Matthew Peter, Curtain, Rob, Quinlan, Sharon, MacMillan, J

Migraine is a multifactorial disorder characterised by headpain, nausea, vomiting, photophobia and often severe, neurological disturbances. Neurotransmitter-related pathways have been the main focus...

Vascular and Hormonal Variants are Implicated in Migraine Susceptibility (2004)

Griffiths, Lyn, Lea, Rodney Arthur, Colson, Natalie Jane, Johnson, Matthew Peter, Curtain, Rob, Quinlan, Sharon Anne, ...

An Investigation of the 5-HT2C Receptor Gene as a Migraine Candidate Gene (2003)

Johnson, Matthew Peter, Lea, Rodney Arthur, Curtain, Rob, MacMillan, John Crichton, Griffiths, Lyn

Migraine is a common complex disorder, currently classified into two main subtypes, migraine with aura (MA) and migraine without aura (MO). The strong preponderance of females to males suggests an...

An Investigation of the 5-HT2C Receptor Gene as a Migraine Candidate Gene (2003)

Johnson, Matthew Peter, Lea, Rodney Arthur, Curtain, Rob, MacMillan, John Crichton, Griffiths, Lyn

Migraine is a common complex disorder, currently classified into two main subtypes, migraine with aura (MA) and migraine without aura (MO). The strong preponderance of females to males suggests an...

An Investigation of the 5-HT2C Receptor Gene as a Migraine Candidate Gene (2003)

Johnson, Matthew Peter, Lea, Rodney Arthur, Curtain, Rob, MacMillan, John Crichton, Griffiths, Lyn

Migraine is a common complex disorder, currently classified into two main subtypes, migraine with aura (MA) and migraine without aura (MO). The strong preponderance of females to males suggests an...

A Typical Migraine Susceptibility Region Localizes to Chromosome 1q31 (2002)

Lea, Rodney Arthur, Shepherd, A.G., Curtain, Rob, Nyholt, D., Quinlan, Sharon, Brimage, P.J., ...

Yes

A Typical Migraine Susceptibility Region Localizes to Chromosome 1q31 (2002)

Lea, Rodney Arthur, Shepherd, A.G., Curtain, Rob, Nyholt, D., Quinlan, Sharon, Brimage, P.J., ...

A Typical Migraine Susceptibility Region Localizes to Chromosome 1q31 (2002)

Lea, Rodney Arthur, Shepherd, A.G., Curtain, Rob, Nyholt, D., Quinlan, Sharon, Brimage, P.J., ...

Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension (2001)

Rutherford, Susan, Johnson, Matthew Peter, Curtain, Rob, Griffiths, Lyn, Not Stated

Yes

Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension (2001)

Rutherford, Susan, Johnson, Matthew Peter, Curtain, Rob, Griffiths, Lyn