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The Euvichol story – Development and licensure of a safe, effective and affordable oral cholera vaccine through global public private partnerships

Vaccine, 2018-10, Vol.36 (45), p.6606-6614

2018

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Safety, efficacy, and immunogenicity of a live, quadrivalent human-bovine reassortant rotavirus vaccine in healthy infants

The Journal of pediatrics, 2004-02, Vol.144 (2), p.184-190

2004

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A randomized, observer-blinded, equivalence trial comparing two variations of Euvichol®, a bivalent killed whole-cell oral cholera vaccine, in healthy adults and children in the Philippines

Vaccine, 2018-07, Vol.36 (29), p.4317-4324

2018

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Immunogenicity of a multi-component recombinant human acrosomal protein vaccine in female Macaca fascicularis

Journal of reproductive immunology, 2008-04, Vol.77 (2), p.126-141

2008

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The natural history and evolution of human and simian T cell leukemia/lymphotropic viruses

Current opinion in genetics & development, 1995-12, Vol.5 (6), p.807-813

1995

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Treatment of chronic hepatitis B in children with prednisone followed by alfa-interferon: a controlled randomized study

Journal of hepatology, 1994-02, Vol.20 (2), p.163-167

1994

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Cytomegalovirus as a co-factor of disease progression in human immunodeficiency virus type 1 infection

International journal of clinical & laboratory research, 1994-06, Vol.24 (2), p.86-89

1994

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Familial aggregation of “apple peel” intestinal atresia and cardiac left‐sided obstructive lesions: A possible causal relationship with NOTCH1 gene mutations

American journal of medical genetics. Part A, 2019-08, Vol.179 (8), p.1570-1574

2019

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Hypoplastic left heart syndrome and 21q22.3 deletion

American journal of medical genetics. Part A, 2015-03, Vol.167A (3), p.579-586

2015

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Small 4p16.3 deletions: Three additional patients and review of the literature

American journal of medical genetics. Part A, 2018-11, Vol.176 (11), p.2501-2508

2018

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Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis

European journal of medical genetics, 2013-02, Vol.56 (2), p.80-87

2013

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Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease

European journal of medical genetics, 2023-01, Vol.66 (1), p.104651-104651, Article 104651

2023

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Left ventricular non compaction with aortic valve anomalies: A recurrent feature of 22q11.2 distal deletion syndrome

European journal of medical genetics, 2015-08, Vol.58 (8), p.406-408

2015

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Copy number variation analysis implicates novel pathways in patients with oculo‐auriculo‐vertebral‐spectrum and congenital heart defects

Clinical genetics, 2021-09, Vol.100 (3), p.268-279

2021

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Behavioral Profile in RASopathies

American journal of medical genetics. Part A, 2014-04, Vol.164A (4), p.934-942

2014

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Gershoni-Baruch syndrome: First report of a surviving child

American journal of medical genetics. Part A, 2016-03, Vol.170A (3), p.707-711

2016

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Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: Rare association with pulmonary valve stenosis

European journal of medical genetics, 2013-03, Vol.56 (3), p.144-149

2013

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Holt-Oram syndrome with intermediate atrioventricular canal defect, and aortic coarctation: Functional characterization of a de novo TBX5 mutation

American journal of medical genetics. Part A, 2014-06, Vol.164A (6), p.1419-1424

2014

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The Euvichol story – Development and licensure of a safe, effective and affordable oral cholera vaccine through global public private partnerships

Safety, efficacy, and immunogenicity of a live, quadrivalent human-bovine reassortant rotavirus vaccine in healthy infants

Protection against cholera from killed whole-cell oral cholera vaccines: a systematic review and meta-analysis

A non-inferiority trial comparing two killed, whole cell, oral cholera vaccines (Cholvax vs. Shanchol) in Dhaka, Bangladesh

A randomized, observer-blinded, equivalence trial comparing two variations of Euvichol®, a bivalent killed whole-cell oral cholera vaccine, in healthy adults and children in the Philippines

Immunogenicity of a multi-component recombinant human acrosomal protein vaccine in female Macaca fascicularis

The natural history and evolution of human and simian T cell leukemia/lymphotropic viruses

Treatment of chronic hepatitis B in children with prednisone followed by alfa-interferon: a controlled randomized study

Cytomegalovirus as a co-factor of disease progression in human immunodeficiency virus type 1 infection

Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair

SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations

Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy

Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: Molecular diversity and associated phenotypic spectrum

Familial aggregation of “apple peel” intestinal atresia and cardiac left‐sided obstructive lesions: A possible causal relationship with NOTCH1 gene mutations

Hypoplastic left heart syndrome and 21q22.3 deletion

Small 4p16.3 deletions: Three additional patients and review of the literature

Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis

Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness

Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease

Left ventricular non compaction with aortic valve anomalies: A recurrent feature of 22q11.2 distal deletion syndrome

Copy number variation analysis implicates novel pathways in patients with oculo‐auriculo‐vertebral‐spectrum and congenital heart defects

Behavioral Profile in RASopathies

Gershoni-Baruch syndrome: First report of a surviving child

Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: Rare association with pulmonary valve stenosis

Holt-Oram syndrome with intermediate atrioventricular canal defect, and aortic coarctation: Functional characterization of a de novo TBX5 mutation

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