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Paramagnetic Phosphametallocenes

Phosphorus, sulfur, and silicon and the related elements, 2002-08, Vol.177 (8-9), p.1999-2000

2002

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Synthesis and Properties of [NiCp(2,5-tBu2PC4H2)], a 20-Valence-Electron Phosphanickelocene

Chemistry : a European journal, 2005-09, Vol.11 (18), p.5381-5390

2005

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Monophospholyl Analogs of Cobaltocenium, Rhodocenium, and Iridocenium Cations. Molecular Structures of [MCp(η 5 -PC4H2tBu2)]+BPh4 - (M = Co, Rh)

Organometallics, 2000-03, Vol.19 (6), p.954-956

2000

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Synthesis and Properties of [CoCp(2,5-PC4tBu2H2)]: The First Monophosphacobaltocene

Chemistry : a European journal, 2003-06, Vol.9 (11), p.2567-2573

2003

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2,5-Di-(tert-butyl)phospholyl sandwich complexes containing group 14 elements (Ge, Sn, Pb). Synthesis, molecular structure, and ring transfer chemistry of [M(PC4H2But2)2] (M= Sn, Pb)

Chemical communications (Cambridge, England), 1999-07 (14), p.1273-1274

1999

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Strengthening Nutrition Interventions in Antenatal Care Services Affects Dietary Intake, Micronutrient Intake, Gestational Weight Gain, and Breastfeeding in Uttar Pradesh, India: Results of a Cluster-Randomized Program Evaluation

The Journal of nutrition, 2021-08, Vol.151 (8), p.2282-2295

2021

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Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 1996-12, Vol.94 (12), p.3069-3073

1996

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First description of germline mosaicism in familial hypertrophic cardiomyopathy

Journal of medical genetics, 2000-02, Vol.37 (2), p.132-134

2000

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Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

Journal of molecular medicine (Berlin, Germany), 1998-03, Vol.76 (3-4), p.208-214

1998

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Apical left ventricular aneurysm without atrio‐ventricular block due to a lamin A/C gene mutation

European journal of heart failure, 2003-12, Vol.5 (6), p.821-825

2003

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Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped population

International journal of cardiology, 2003-07, Vol.90 (1), p.33-38

2003

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Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathy

European heart journal, 2005-09, Vol.26 (18), p.1882-1886

2005

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Genomic Organisation, Alternative Splicing and Polymorphisms of the Human Cardiac Troponin T Gene

Journal of molecular and cellular cardiology, 1998-06, Vol.30 (6), p.1247-1253

1998

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Kinetics and mechanism studies of the catalytic dehydrogenation of isobutane on Platinum-Indium catalyst

Studies in Surface Science and Catalysis, 1999, Vol.122, p.367-374

1999

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Effect of coke deposition on catalyst texture during catalytic cracking reaction

Characterization of Porous Solids VI, 2002, Vol.144, p.451-458

2002

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Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation

Archives des maladies du coeur et des vaisseaux, 2005-01, Vol.98 (1), p.67

2005

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Diagnostic value of a two-dimensional echocardiographic score for left ventricular hypertrophy validated by the Imatron CT scan in familial hypertrophic cardiomyopathy

Archives des maladies du coeur et des vaisseaux, 2006-10, Vol.99 (10), p.877

2006

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151 Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation

European journal of heart failure. Supplements, 2003-06, Vol.2 (Suppl_1), p.26-26

2003

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Paramagnetic Phosphametallocenes

Synthesis and Properties of [NiCp(2,5-tBu2PC4H2)], a 20-Valence-Electron Phosphanickelocene

Monophospholyl Analogs of Cobaltocenium, Rhodocenium, and Iridocenium Cations. Molecular Structures of [MCp(η 5 -PC4H2tBu2)]+BPh4 - (M = Co, Rh)

Synthesis and Properties of [CoCp(2,5-PC4tBu2H2)]: The First Monophosphacobaltocene

2,5-Di-(tert-butyl)phospholyl sandwich complexes containing group 14 elements (Ge, Sn, Pb). Synthesis, molecular structure, and ring transfer chemistry of [M(PC4H2But2)2] (M= Sn, Pb)

Strengthening Nutrition Interventions in Antenatal Care Services Affects Dietary Intake, Micronutrient Intake, Gestational Weight Gain, and Breastfeeding in Uttar Pradesh, India: Results of a Cluster-Randomized Program Evaluation

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy

First description of germline mosaicism in familial hypertrophic cardiomyopathy

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

Apical left ventricular aneurysm without atrio‐ventricular block due to a lamin A/C gene mutation

Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped population

Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathy

Genomic Organisation, Alternative Splicing and Polymorphisms of the Human Cardiac Troponin T Gene

Kinetics and mechanism studies of the catalytic dehydrogenation of isobutane on Platinum-Indium catalyst

Effect of coke deposition on catalyst texture during catalytic cracking reaction

Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation

Diagnostic value of a two-dimensional echocardiographic score for left ventricular hypertrophy validated by the Imatron CT scan in familial hypertrophic cardiomyopathy

151 Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation

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