Juan Carlos López‐Gutiérrez

Author

Also Known As

J C Lopez, J C Lopez Gutierrez, J C Lopez-Gutierrez, J C López, J C López Gutierrez, J C López Gutiérrez, J C López Gutíerrez, J C López Gútiérrez, J C López-Gutiérrez, J. C. Lopez Gutierrez

305

Publications

5.4K

Citations

H-Index

Concepts

All Affiliations

Hospital Universitario La Paz Centre for Biomedical Network Research on Rare Diseases Instituto de Salud Carlos III Hospital Universitario Virgen del Rocío Universidad Autónoma de Madrid

About

Juan Carlos López‐Gutiérrez is an author at Hospital Universitario La Paz specializing in medicine, pathology, and surgery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	26	1.1K
2	Health Sciences	2	2	85
3	Anatomy	2	2	193
4	Education	1	1	10
5	Public Health	1	1	61

Juan Carlos López‐Gutiérrez

Publications

Citations

H-Index

Page 1

	Year	Citations
A Randomized, Controlled Trial of Oral Propranolol in Infantile Hemangioma Christine Léauté-Labrèze, Peter H. Hoeger, J. Mazereeuw‐Hautier, New England Journal of Medicine	2015	745
Sirolimus in the Treatment of Vascular Anomalies Mariela Dore, V Núñez Cerezo, Manuel Cervantes, European Journal of Pediatric Surgery	2016	217
Consensus Document of the International Union of Angiology (IUA)-2013. Current concept on the management of arterio-venous management. B B Lee, Iris Baumgärtner, H.-P. Berlien, PubMed Arterio-venous ManagementDiagnosisPathologyVascular MalformationArterio-venous Malformations	2013	181
Somatic activating mutations in <i>PIK3CA</i> cause generalized lymphatic anomaly Lara Rodríguez‐Laguna, Noelia Agrá, Kristina Ibáñez, The Journal of Experimental Medicine	2018	140
Propranolol for Infantile Hemangiomas Lorea Bagazgoitia, Antonio Torrelo, Juan Carlos López‐Gutiérrez, Pediatric Dermatology	2011	103
Biliary atresia and the polysplenia syndrome: Its impact on final outcome J. Vázquez, Juan Carlos López‐Gutiérrez, M Gámez, Journal of Pediatric Surgery OphthalmologyBiliary TractPathologyPolysplenia SyndromeBiliary Disorder	1995	82
Multidisciplinary guidelines for initial evaluation of complicated lymphatic anomalies—expert opinion consensus Ionela Iacobas, Denise M. Adams, Sheena Pimpalwar, Pediatric Blood & Cancer	2019	80
CLAPO syndrome: identification of somatic activating PIK3CA mutations and delineation of the natural history and phenotype Lara Rodríguez‐Laguna, Kristina Ibáñez, Gema Gordo, Genetics in Medicine Developmental BiologyGenetic DisorderGeneticsNatural HistoryClapo Syndrome	2018	78
Long-term outcome of vincristine-aspirin-ticlopidine (VAT) therapy for vascular tumors associated with kasabach-merritt phenomenon Israel Fernández‐Pineda, Juan Carlos López‐Gutiérrez, Gloria Chocarro, Pediatric Blood & Cancer	2013	72
Alpelisib for treatment of patients with PIK3CA-related overgrowth spectrum (PROS) Guillaume Canaud, Juan Carlos López‐Gutiérrez, Alan D. Irvine, Genetics in Medicine OncologyMedicinePathologyPharmacologyRadiation Oncology	2023	70

Page 1