Héctor M. Targovnik

Author

Héctor M. Targovnik

Also Known As

H M Targovnik, H Targovnik, H. M. Targovnik, H. Targovnik, H.M. Targovnik, HECTOR M. TARGOVNIK, HECTOR TARGOVNIK, HM Targovnik, Hector M Targovnik, Hector M. TARGOVNIK

163

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Universidad de Buenos Aires Hospital de Clínicas "José de San Martín"Consejo Nacional de Investigaciones Científicas y Técnicas Universidad de Salamanca Hospital General de Niños Ricardo Gutierrez

About

Héctor M. Targovnik is an author at Universidad de Buenos Aires specializing in medicine, genetics, and thyroid disorders.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	35	1.5K
2	Natural Sciences	9	9	262
3	Public Health	8	8	227
4	Engineering	3	3	63
5	Allergy	1	1	19

Héctor M. Targovnik

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter. Marc Abramowicz, Héctor M. Targovnik, Viviana Varela, Journal of Clinical Investigation BiologyMendelian DisorderGenetic DisorderGeneticsIodine Deficiency Disorders	1992	192
A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism. Tamio Ieiri, Pascale Cochaux, Héctor M. Targovnik, Journal of Clinical Investigation Thyroglobulin GeneGeneticsMolecular BiologyMolecular GeneticsCongenital Goiter	1991	169
Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones. Geraldo Medeiros‐Neto, Pan Suk Kim, Sung Eun Yoo, Journal of Clinical Investigation Molecular ChaperonesDevelopmental BiologyCongenital Hypothyroid GoiterDeficient ThyroglobulinGenetics	1996	132
An unusually long poly(purine)-poly(pyrimidine) sequence is located upstream from the human thyroglobulin gene Daniel Christophe, Bartolomé Cabrer, Albino Bacolla, Nucleic Acids Research	1985	118
Control of dendritic cell maturation and function by triiodothyronine Iván Mascanfroni, María M. Montesinos, Sebastián Susperreguy, The FASEB Journal	2007	87
A Premature Stopcodon in Thyroglobulin Messenger RNA Results in Familial Goiter and Moderate Hypothyroidism Simone A. R. van de Graaf, Carrie Ris‐Stalpers, Geertruda J. M. Veenboer, The Journal of Clinical Endocrinology & Metabolism GeneticsMolecular BiologyThyroid GlandMolecular GeneticsParathyroid Gland	1999	85
Compound Heterozygous Mutations in the Thyroglobulin Gene (1143delC and 6725G→A [R2223H]) Resulting in Fetal Goitrous Hypothyroidism Philippe Caron, Christian M. Moya, David Malet, The Journal of Clinical Endocrinology & Metabolism Thyroglobulin GeneGeneticsFetal MedicineGynecologyMolecular Genetics	2003	80
A nonsense mutation causes human hereditary congenital goiter with preferential production of a 171-nucleotide-deleted thyroglobulin ribonucleic acid messenger. Héctor M. Targovnik, Geraldo Medeiros‐Neto, Viviana Varela, The Journal of Clinical Endocrinology & Metabolism GeneticsPreferential ProductionMolecular BiologyPathologyMolecular Genetics	1993	78
Three Mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A&gt;C) in the Dual Oxidase 2 Gene Responsible for Congenital Goiter and Iodide Organification Defect Viviana Varela, Sebastián Esperante, Laura Gruñeiro‐Papendieck, Clinical Chemistry	2005	65
Viability and infectiousness of eggs of Echinococcus granulosus aged under natural conditions of inferior arid climate Paula Sánchez Thevenet, Oscar Jensen, Ricardo Drut, Veterinary Parasitology Natural ConditionsEchinococcus GranulosusInferior Arid ClimateMicrobiologyMedicine	2005	64

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