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The natural history of Noonan syndrome: a long-term follow-up study

Archives of disease in childhood, 2007-02, Vol.92 (2), p.128-132

2007

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Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish

Heart (British Cardiac Society), 2008-10, Vol.94 (10), p.1326-1330

2008

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Homozygous Mutation of Desmocollin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy with Mild Palmoplantar Keratoderma and Woolly Hair

Cardiology, 2009-03, Vol.113 (1), p.28-34

2009

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CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis

Clinical genetics, 2012-02, Vol.81 (2), p.191-197

2012

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Supply Chain Management in Vegetables

Paripex - Indian Journal Of Research, 2012-01, Vol.3 (2), p.315-316

2012

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A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1–12q14

Journal of medical genetics, 2005-01, Vol.42 (1), p.80-82

2005

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Mutations in PTPN11 , encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

Nature genetics, 2001-12, Vol.29 (4), p.465-468

2001

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Acute and preventive treatment use in a phase-3 randomized trial of galcanezumab in chronic cluster headache

Journal of the neurological sciences, 2019-10, Vol.405, p.62-63

2019

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PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

American journal of human genetics, 2002-06, Vol.70 (6), p.1555-1563

2002

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Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype

Journal of medical genetics, 2011-04, Vol.48 (4), p.251-255

2011

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Health and Position Tracking for Mountain Climbers

2023 9th International Conference on Advanced Computing and Communication Systems (ICACCS), 2023, Vol.1, p.2052-2056

2023

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IEEE_Xplore

Influence of stir casting route process parameters in fabrication of aluminium matrix composites – A review

Materials today : proceedings, 2021, Vol.45, p.6660-6664

2021

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Composite Wear Actions of Glass Fiber Reinforced Titanates Filled Epoxy Resin

International journal of recent technology and engineering, 2020-09, Vol.9 (3), p.642-647

2020

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Association of interleukin-6 -174G/C promoter polymorphism with hypertension and left ventricular hypertrophy in dialysis patients

Kidney international, 2003-08, Vol.64 (2), p.616-622

2003

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Medical marijuana in neurology

Expert review of neurotherapeutics, 2014-12, Vol.14 (12), p.1453-1465

2014

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A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

Nature genetics, 1998-10, Vol.20 (2), p.143-148

1998

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Triptan Education and Improving Knowledge for Optimal Migraine Treatment: An Observational Study

Headache, 2014-04, Vol.54 (4), p.686-697

2014

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Paternal Germline Origin and Sex-Ratio Distortion in Transmission of PTPN11 Mutations in Noonan Syndrome

American journal of human genetics, 2004-09, Vol.75 (3), p.492-497

2004

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A Mutation in VEGFC, a Ligand for VEGFR3, is Associated with Autosomal Dominant Milroy-like Primary Lymphedema

Circulation research, 2013, Vol.112 (6)

2013

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Mapping of the human insulin receptor substrate-2 gene, identification of a linked polymorphic marker and linkage analysis in families with Type II diabetes : no evidence for a major susceptibility role

Diabetologia, 1998-11, Vol.41 (11), p.1389-1391

1998

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CD14 C(-260) T promoter polymorphism and prevalence of acute coronary syndromes

International journal of cardiology, 2005-02, Vol.98 (2), p.307-312

2005

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Polymorphism of renin–angiotensin system genes in dialysis patients—association with cerebrovascular disease

Nephrology, dialysis, transplantation, 2002-12, Vol.17 (12), p.2184-2188

2002

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Different mutations in the NF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS)

American journal of medical genetics, 2003-05, Vol.119A (1), p.1-8

2003

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Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome

Human genetics, 2002-10, Vol.111 (4-5), p.421-427

2002

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Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11

Journal of human genetics, 2005, Vol.50 (1), p.21-25

2005

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The natural history of Noonan syndrome: a long-term follow-up study

Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish

Homozygous Mutation of Desmocollin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy with Mild Palmoplantar Keratoderma and Woolly Hair

CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis

Supply Chain Management in Vegetables

A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1–12q14

Mutations in PTPN11 , encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

Acute and preventive treatment use in a phase-3 randomized trial of galcanezumab in chronic cluster headache

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype

Health and Position Tracking for Mountain Climbers

Influence of stir casting route process parameters in fabrication of aluminium matrix composites – A review

Composite Wear Actions of Glass Fiber Reinforced Titanates Filled Epoxy Resin

Association of interleukin-6 -174G/C promoter polymorphism with hypertension and left ventricular hypertrophy in dialysis patients

Medical marijuana in neurology

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

Triptan Education and Improving Knowledge for Optimal Migraine Treatment: An Observational Study

Paternal Germline Origin and Sex-Ratio Distortion in Transmission of PTPN11 Mutations in Noonan Syndrome

A Mutation in VEGFC, a Ligand for VEGFR3, is Associated with Autosomal Dominant Milroy-like Primary Lymphedema

Mapping of the human insulin receptor substrate-2 gene, identification of a linked polymorphic marker and linkage analysis in families with Type II diabetes : no evidence for a major susceptibility role

CD14 C(-260) T promoter polymorphism and prevalence of acute coronary syndromes

Polymorphism of renin–angiotensin system genes in dialysis patients—association with cerebrovascular disease

Different mutations in the NF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS)

Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome

Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11

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