Pablo
Prieto Matos
Profesor Permanente Laboral
Hospital Universitario de Salamanca
Salamanca, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario de Salamanca (21)
2024
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PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patients
Child's Nervous System
2023
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Adaptation, reliability and validity of health-related quality of life questionnaires: Disabkids chronic and specific diabetes disease in children and adolescents with diabetes mellitus type 1
Endocrinologia, Diabetes y Nutricion, Vol. 70, pp. 18-26
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Clinical description, molecular delineation and genotype-phenotype correlation in 340 patients with KBG syndrome: Addition of 67 new patients
Journal of Medical Genetics, Vol. 60, Núm. 7, pp. 644-654
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Crisis neonatales y evolución a epilepsia en un hospital de tercer nivel
Revista de neurologia, Vol. 77, Núm. 10, pp. 249-252
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Immune stress suppresses innate immune signaling in preleukemic precursor B-cells to provoke leukemia in predisposed mice
Nature Communications, Vol. 14, Núm. 1
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Lessons from mouse models in the impact of risk factors on the genesis of childhood B-cell leukemia
Frontiers in Immunology
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Rango normal de subunidad ácido-lábil (ALS) en niños españoles y su relación con la edad, el sexo, el estadio puberal y otros factores de crecimiento
Anales de Pediatria, Vol. 98, Núm. 5, pp. 329-337
2022
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Childhood B-Cell Preleukemia Mouse Modeling
International Journal of Molecular Sciences, Vol. 23, Núm. 14
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Transient Inhibition of the JAK/STAT Pathway Prevents B-ALL Development in Genetically Predisposed Mice
Cancer research, Vol. 82, Núm. 6, pp. 1098-1109
2018
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Autosomal recessive hypercholesterolemia in Spain
Atherosclerosis, Vol. 269, pp. 1-5
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Clinical response to growth hormone in children with intrauterine growth retardation without catch-up growth in Castilla y León (Spain)
Endocrinologia, Diabetes y Nutricion, Vol. 65, Núm. 10, pp. 584-591
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Heterozygous aggrecan variants are associated with short stature and brachydactyly: Description of 16 probands and a review of the literature
Clinical Endocrinology, Vol. 88, Núm. 6, pp. 820-829
2017
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Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia
Clinical Genetics, Vol. 92, Núm. 1, pp. 91-98
2016
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Analysis of FOXP3 gene in children with allergy and autoimmune diseases
Allergologia et Immunopathologia, Vol. 44, Núm. 1, pp. 32-40
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Clinical and molecular characteristics of homozygous familial hypercholesterolemia patients: Insights from SAFEHEART registry
Journal of Clinical Lipidology, Vol. 10, Núm. 4, pp. 953-961
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Epiphysiolysis and recombinant growth hormone
Anales de Pediatria, Vol. 84, Núm. 4, pp. 239-240
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Image in clinical pediatrics. Make your diagnosis: Hidden bone dysplasia
Pediatria Integral
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Síndrome de Turner: análisis de 42 casos
Medicina Clinica, Vol. 147, Núm. 8, pp. 348-351
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Tratamiento con hormona de crecimiento en 2 pacientes con deleción 22q11.21
Medicina Clinica
2014
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Defecto congénito del arco posterior del atlas
Emergencias