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A simulation model estimates lifetime health and economic outcomes of screening prediabetes using the 1-h plasma glucose.
- Published in:
- Acta Diabetologica, 2023, v. 60, n. 1, p. 9, doi. 10.1007/s00592-022-01963-3
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- Publication type:
- Article
Osteopontin in the Cerebrospinal Fluid of Patients with Severe Aneurysmal Subarachnoid Hemorrhage.
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- Cells (2073-4409), 2019, v. 8, n. 7, p. 695, doi. 10.3390/cells8070695
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- Publication type:
- Article
Exercise Influence on Hippocampal Function: Possible Involvement of Orexin-A.
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- Frontiers in Physiology, 2017, v. 8, p. 1, doi. 10.3389/fphys.2017.00085
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- Article
Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients.
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- Nutrients, 2017, v. 9, n. 7, p. 783, doi. 10.3390/nu9070783
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- Publication type:
- Article
Quality of life in overweight (obese) and normal-weight women with polycystic ovary syndrome.
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- Patient Preference & Adherence, 2017, p. 423, doi. 10.2147/PPA.S119180
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- Publication type:
- Article
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology.
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- Journal of Bone & Mineral Research, 2020, v. 35, n. 10, p. 1974, doi. 10.1002/jbmr.3993
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- Article
The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone.
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- Journal of Bone & Mineral Research, 2020, v. 35, n. 8, p. 1387, doi. 10.1002/jbmr.3964
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- Publication type:
- Article
Clinical Characteristics and Evolution of Giant Cell Tumor Occurring in Paget's Disease of Bone.
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- Journal of Bone & Mineral Research, 2015, v. 30, n. 2, p. 257, doi. 10.1002/jbmr.2349
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- Publication type:
- Article
Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease.
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- Journal of Bone & Mineral Research, 2013, v. 28, n. 11, p. 2338, doi. 10.1002/jbmr.1975
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- Publication type:
- Article
Giant cell tumor occurring in familial Paget's disease of bone: Report of clinical characteristics and linkage analysis of a large pedigree.
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- Journal of Bone & Mineral Research, 2013, v. 28, n. 2, p. 341, doi. 10.1002/jbmr.1750
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- Publication type:
- Article
A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's disease.
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- Journal of Bone & Mineral Research, 2012, v. 27, n. 2, p. 443, doi. 10.1002/jbmr.542
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- Publication type:
- Article
SQSTM1 Gene Analysis and Gene-Environment Interaction in Paget's Disease of Bone.
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- Journal of Bone & Mineral Research, 2010, v. 25, n. 6, p. 1375, doi. 10.1002/jbmr.31
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- Publication type:
- Article
A novel diagnostic method to detect truncated neurofibromin in neurofibromatosis 1.
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- Journal of Neurochemistry, 2015, v. 135, n. 6, p. 1123, doi. 10.1111/jnc.13396
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- Publication type:
- Article
Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population.
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- Indian Journal of Otolaryngology & Head & Neck Surgery, 2014, v. 66, n. 3, p. 297, doi. 10.1007/s12070-014-0706-6
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- Publication type:
- Article
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts.
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- Neurogenetics, 2008, v. 9, n. 1, p. 25, doi. 10.1007/s10048-007-0109-x
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- Publication type:
- Article
OP52 Health Technology Assessment Of Pain-Free Blood Draw Devices In Pediatrics.
- Published in:
- International Journal of Technology Assessment in Health Care, 2022, v. 38, p. S20, doi. 10.1017/S0266462322001064
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- Publication type:
- Article
Occult knowledge and sacred geometry: A new interpretation of a portrait of Rubens and his son from the Hermitage Museum.
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- De Zeventiende Eeuw, 2017, v. 32, n. 2, p. 211, doi. 10.18352/dze.10130
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- Publication type:
- Article
Occult knowledge and sacred geometry.
- Published in:
- De Zeventiende Eeuw, 2016, v. 32, n. 2, p. 211, doi. 10.18352/dze.10130
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- Publication type:
- Article
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3654, doi. 10.1093/hmg/ddt215
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- Publication type:
- Article
Osteopontin: Relation between Adipose Tissue and Bone Homeostasis.
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- Stem Cells International, 2017, p. 1, doi. 10.1155/2017/4045238
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- Publication type:
- Article
Association of a GRIA3 Gene Polymorphism With Migraine in an Australian Case-Control Cohort.
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- Headache: The Journal of Head & Face Pain, 2013, v. 53, n. 8, p. 1245, doi. 10.1111/head.12151
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- Publication type:
- Article
Circulating Extracellular Vesicles in Subarachnoid Hemorrhage Patients: Characterization and Cellular Effects.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 19, p. 14913, doi. 10.3390/ijms241914913
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- Publication type:
- Article
Rare Variants in Autophagy and Non-Autophagy Genes in Late-Onset Pompe Disease: Suggestions of Their Disease-Modifying Role in Two Italian Families.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3625, doi. 10.3390/ijms22073625
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- Publication type:
- Article
Bone Turnover and the Osteoprotegerin–RANKL Pathway in Tumor-Induced Osteomalacia: A Longitudinal Study of Five Cases.
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- Calcified Tissue International, 2009, v. 85, n. 4, p. 293, doi. 10.1007/s00223-009-9275-1
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- Article
Vitamin D receptor gene polymorphisms predict acquired resistance to clodronate treatment in patients with Paget's disease of bone.
- Published in:
- 2008
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- Publication type:
- journal article
Whole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian Population.
- Published in:
- Frontiers in Neurology, 2020, v. 10, p. 1, doi. 10.3389/fneur.2019.01362
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- Publication type:
- Article
Exercise Modifies the Gut Microbiota with Positive Health Effects.
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- Oxidative Medicine & Cellular Longevity, 2017, p. 1, doi. 10.1155/2017/3831972
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- Publication type:
- Article
Molecular analysis of the mature T cell proliferation-1 (MTCP-1) gene in Xq28-linked incontinentia pigmenti.
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- European Journal of Human Genetics, 2000, v. 8, n. 4, p. 239, doi. 10.1038/sj.ejhg.5200454
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- Publication type:
- Article
FSHR gene polymorphisms influence bone mineral density and bone turnover in postmenopausal women.
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- European Journal of Endocrinology, 2010, v. 163, n. 1, p. 165, doi. 10.1530/EJE-10-0043
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- Publication type:
- Article
Imerslund-Gräsbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN.
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- 2013
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- Publication type:
- Journal Article
Imerslund-Gräsbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN.
- Published in:
- Italian Journal of Pediatrics, 2013, v. 39, n. 1, p. 58, doi. 10.1186/1824-7288-39-58
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- Publication type:
- Article
The identification of H3F3A mutation in giant cell tumour of the clivus and the histological diagnostic algorithm of other clival lesions permit the differential diagnosis in this location.
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- 2018
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- Publication type:
- journal article
The melatonin receptor 1A (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis.
- Published in:
- Nephrology Dialysis Transplantation, 2012, v. 27, n. 1, p. 210, doi. 10.1093/ndt/gfr216
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- Publication type:
- Article
683.Adenoviral Vector-Mediated Expression of Bone Morphogenetic Protein-4 in Mesenchymal Stem Cells Induces Differentiation into the Osteoblastic Lineage and Bone Production In Vivo
- Published in:
- 2005
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- Publication type:
- Abstract
Role of Autonomic Nervous System and Orexinergic System on Adipose Tissue.
- Published in:
- Frontiers in Physiology, 2017, v. 8, p. 1, doi. 10.3389/fphys.2017.00137
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- Publication type:
- Article
Thirty years of SET/TAF1β/I2PP2A: from the identification of the biological functions to its implications in cancer and Alzheimer's disease.
- Published in:
- Bioscience Reports, 2022, v. 42, n. 11, p. 1, doi. 10.1042/BSR20221280
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- Publication type:
- Article
ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses.
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- Neurological Sciences, 2008, v. 29, n. 2, p. 113, doi. 10.1007/s10072-008-0870-0
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- Publication type:
- Article
The Role of New Morphological Parameters Provided by the BC 6800 Plus Analyzer in the Early Diagnosis of Sepsis.
- Published in:
- Diagnostics (2075-4418), 2024, v. 14, n. 3, p. 340, doi. 10.3390/diagnostics14030340
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- Publication type:
- Article
Cerrado and Pantanal fruit flours affect gut microbiota composition in healthy and post‐COVID‐19 individuals: an in vitro pilot fermentation study.
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- International Journal of Food Science & Technology, 2023, v. 58, n. 8, p. 4495, doi. 10.1111/ijfs.16274
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- Publication type:
- Article
Effects of low-carbohydrate diet therapy in overweight subjects with autoimmune thyroiditis: possible synergism with ChREBP.
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- Drug Design, Development & Therapy, 2016, v. 10, p. 2939, doi. 10.2147/DDDT.S106440
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- Publication type:
- Article
piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene.
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- PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0022727
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- Publication type:
- Article
Aumentare la consapevolezza delle decisioni in ambito sanitario: il metodo Decision-oriented HTA.
- Published in:
- Giornale Italiano di Health Technology Assessment Delivery, 2021, v. 14, n. 3, p. 1
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- Publication type:
- Article
Analysis of Genetic and Non-genetic Predictors of Levodopa Induced Dyskinesia in Parkinson's Disease.
- Published in:
- Frontiers in Pharmacology, 2021, v. 11, p. N.PAG, doi. 10.3389/fphar.2021.640603
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- Publication type:
- Article
Novel autophagic vacuolar myopathies: Phenotype and genotype features.
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- Neuropathology & Applied Neurobiology, 2021, v. 47, n. 5, p. 664, doi. 10.1111/nan.12690
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- Publication type:
- Article
Basal Forebrain Cholinergic System and Orexin Neurons: Effects on Attention.
- Published in:
- Frontiers in Behavioral Neuroscience, 2017, v. 11, p. 1, doi. 10.3389/fnbeh.2017.00010
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- Publication type:
- Article
Familial recurrence of congenital heart disease in patients with ostium secundum atrial septal defect.
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- European Heart Journal, 2005, v. 26, n. 20, p. 2179, doi. 10.1093/eurheartj/ehi378
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- Publication type:
- Article
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-159
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- Publication type:
- Article
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-91
- By:
- Publication type:
- Article
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy.
- Published in:
- 2013
- By:
- Publication type:
- journal article