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PubPharm (466)

1

Intensified epidemiological surveillance of arbovirosis : First case of native dengue fever in Catalonia (Spain), Northern Metropolitan Area of Barcelona, 2018-2019

enthalten in: Atencion primaria | 2021

von Valerio, L. | Roure Díez, S. | Benítez, R. | +6

2

Pulmonary arteriovenous fistulas in a pediatric patient : a case report

enthalten in: Archivos argentinos de pediatria | 2020

von Samboni, Y. | Tordecilla, L. | Acuña, G. | +1

3

Sjögren-Larsson syndrome : Pediatric case report

enthalten in: Archivos argentinos de pediatria | 2018

von García-Ortiz, L. | Gómez-López, R. | Rivera-Pedroza, C. | +3

4

Association between central diabetes insipidus and type 2 diabetes mellitus

enthalten in: Medicina | 2018

von Palumbo, C. | Nicolaci, N. | La Manna, A. | +2

5

Pseudopseudohypoparathyroidism vs progressive osseous heteroplasia in absence of family history

enthalten in: Medicina clinica | 2015

von Pereda, A. | González Oliva, E. | Riaño-Galán, I. | +1

ErratumIn: Med Clin (Barc). 2017 Feb 23;148(4):194. - PMID 28073519

6

Nosocomial infection due to Trichosporon asahii in a critical burned patient

enthalten in: Revista iberoamericana de micologia | 2015

von Tamayo Lomas, L. | Domínguez-Gil González, M. | Martín Luengo, A. | +2

7

Isolation of Staphylococcus aureus hetero-resistant to vancomycin (hVISA) in the Regional Hospital of Concepción, Chile

enthalten in: Revista chilena de infectologia : organo oficial de la Sociedad Chilena de Infectologia | 2015

von Vega, F. | Alarcón, P. | Domínguez, M. | +5

8

Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

enthalten in: Revista de neurologia | 2015

von Quintela, I. | Barros-Angueira, F. | Perez-Gay, L. | +4

9

Stereotactic aspiration of Spirometra mansonides larvae

enthalten in: Revista chilena de infectologia : organo oficial de la Sociedad Chilena de Infectologia | 2015

von Caballero, J. | Morales, L. | García, D. | +3

10

Usefulness of a diagnostic algorithm hyperferritinemia : A case report of a Spanish family with hereditary hemochromatosis and mutation in SLC40A1 gene

enthalten in: Medicina clinica | 2015

von Vargas, J. | Muñoz, A. | Samper, B. | +1

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