Pablo Sanjurjo

Hospital de Cruces — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

21h-index1.6kcitations109works0.02yr avg
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Research Topics

Metabolism and Genetic Disorders(40), Fatty Acid Research and Health(28), Diet and metabolism studies(14), Birth, Development, and Health(11), Amino Acid Enzymes and Metabolism(11)

Publications107 total

Diagnosis features of pediatric Gaucher disease patients in the era of enzymatic therapy, a national-base study from the Spanish Registry of Gaucher Disease
Orphanet Journal of Rare Diseases·2017· 44 citedOpen Access
Los medios de comunicación y el tatuaje contemporáneo
Communication & Society·2016Open Access
Media and contemporary tattoo
Communication & Society·2016· 11 citedOpen Access
Recomendaciones para el diagnóstico y el tratamiento de la enfermedad de Gaucher durante la infancia
Acta pediátrica española/Acta pediátrica española·2016· 1 cited
Effects of Maternal Ω‐3 Supplementation on Fatty Acids and on Visual and Cognitive Development
Journal of Pediatric Gastroenterology and Nutrition·2015· 60 cited
Long Term Outcomes of ERT in Children with Gaucher Disease. Spanish Experience
Blood·2014
Arginine-guanidinoacetate-creatine pathway in preterm newborns: creatine biosynthesis in newborns
Journal of Pediatric Endocrinology and Metabolism·2012· 9 citedOpen Access
Reliability of a visual test for the rapid detection of mucopolysaccharidoses: GAG-test®
Journal of Clinical Laboratory Analysis·2011· 11 cited
Fatty acid profile in patients with phenylketonuria and its relationship with bone mineral density
Journal of Inherited Metabolic Disease·2010· 56 cited
Methylation cycle, arginine-creatine pathway and asymmetric dimethylarginine in paediatric renal transplant
Nephrology Dialysis Transplantation·2010· 21 citedOpen Access
Actualización, recomendaciones y consenso sobre el papel de los ácidos grasos poliinsaturados de cadena larga en la gestación, lactancia y primer año de vida
Medicina Clínica·2010· 5 cited
Semen quality at cryobanking before oncologic treatment
2010
Representación mediante arquetipos y generación dirigida por modelo de guías clínicas ejecutables.
JISBD·2010
Update of knowledge, recommendations and full consensus about the role of long chain polyunsaturated fatty acids in pregnancy, lactating period and first year of life
Medicina Clínica·2010· 3 cited
Towards an Effective Knowledge Translation of Clinical Guidelines and Complementary Information
Advances in intelligent and soft computing·2010· 5 cited
Persistence of Essential Fatty Acid Deficiency in Cystic Fibrosis Despite Nutritional Therapy
Pediatric Research·2009· 58 citedOpen Access
Guía clínica de diagnóstico y tratamiento urgente de hiperamonemia neonatal
Anales de Pediatría·2009· 8 cited
Acidemia metilmalónica: causa emergente de enfermedad renal crónica
Gaceta Médica de Bilbao·2009Open Access
Determination of creatine and guanidinoacetate by GC-MS
Clinical Biochemistry·2008· 13 cited
Visual test for detection of pathological glycosaminoglycans excretion in mucopolysaccharidoses. A diagnostic tool in paediatric rheumatology
Pediatric Rheumatology·2008Open Access
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Frequent Co-authors

Luis Aldámiz‐Echevarría(17), José Ignacio Ruiz-Sanz(12), Fernando Andrade(12), Juan Rodríguez‐Soriano(12), Javier Elorz(10), Roberto Matorras(9), Lourdes Perteagudo(9), José Angel Prieto(8), Alfredo Vallo(6), Sergio Lage(5), José Ángel Prieto(5), Vicente Rubio(4), Mireia Aguirre(4), Gustavo Pérez de Nanclares(4), Mercedes Martínez‐Pardo(3), A Baldellou(3), S. Martín Martín(3), María L. Couce(3), Lourdes R. Desviat(2), Belén Pérez(2)