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Osteoporosis in β-thalassaemia major patients: analysis of the genetic background.
- Published in:
- British Journal of Haematology, 2000, v. 111, n. 2, p. 461, doi. 10.1046/j.1365-2141.2000.02382.x
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- Publication type:
- Article
Integrative genomic analyses identify neuroblastoma risk genes involved in neuronal differentiation.
- Published in:
- Human Genetics, 2024, v. 143, n. 11, p. 1293, doi. 10.1007/s00439-024-02700-2
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- Publication type:
- Article
A predicted functional single-nucleotide polymorphism of bone morphogenetic protein-4 gene affects mRNA expression and shows a significant association with cutaneous melanoma in Southern Italian population.
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- Journal of Cancer Research & Clinical Oncology, 2009, v. 135, n. 12, p. 1799, doi. 10.1007/s00432-009-0628-y
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- Publication type:
- Article
Beyond Inflammaging: The Impact of Immune System Aging on Age-Related Muscle Decline, Results From the InCHIANTI Study.
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- Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2024, v. 79, n. 2, p. 1, doi. 10.1093/gerona/glad238
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- Publication type:
- Article
Adapted physical activity and therapeutic exercise in late-onset Pompe disease (LOPD): a two-step rehabilitative approach.
- Published in:
- 2020
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- Publication type:
- journal article
Pain Management in Knee Osteoarthritis: Insights from an Exploratory Online Survey of Italian Patients and Physicians.
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- Healthcare (2227-9032), 2024, v. 12, n. 20, p. 2077, doi. 10.3390/healthcare12202077
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- Publication type:
- Article
Unraveling the joints: a narrative review of osteoarthritis.
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- European Review for Medical & Pharmacological Sciences, 2024, v. 28, n. 15, p. 4080
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- Publication type:
- Article
Genetic Analysis of the Coronavirus SARS-CoV-2 Host Protease TMPRSS2 in Different Populations.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.00872
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- Publication type:
- Article
Galectin-1 is a major effector of TrkB-mediated neuroblastoma aggressiveness.
- Published in:
- Oncogene, 2009, v. 28, n. 19, p. 2015, doi. 10.1038/onc.2009.70
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- Publication type:
- Article
Phosphorylation of nm23-H1 by CKI induces its complex formation with h-prune and promotes cell motility.
- Published in:
- Oncogene, 2008, v. 27, n. 13, p. 1853, doi. 10.1038/sj.onc.1210822
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- Publication type:
- Article
Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias.
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- Frontiers in Physiology, 2020, v. 11, p. N.PAG, doi. 10.3389/fphys.2020.613559
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- Publication type:
- Article
Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein.
- Published in:
- 2020
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- Correction Notice
Correction: Vassallo et al. Hyaluronic Acid-Based Injective Medical Devices: In Vitro Characterization of Novel Formulations Containing Biofermentative Unsulfated Chondroitin or Extractive Sulfated One with Cyclodextrins. Pharmaceuticals 2023, 16 , 1429.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Hyaluronic Acid-Based Injective Medical Devices: In Vitro Characterization of Novel Formulations Containing Biofermentative Unsulfated Chondroitin or Extractive Sulfated One with Cyclodextrins.
- Published in:
- Pharmaceuticals (14248247), 2023, v. 16, n. 10, p. 1429, doi. 10.3390/ph16101429
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- Publication type:
- Article
Mn-loaded apoferritin: a highly sensitive MRI imaging probe for the detection and characterization of hepatocarcinoma lesions in a transgenic mouse model.
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- Contrast Media & Molecular Imaging, 2012, v. 7, n. 3, p. 281, doi. 10.1002/cmmi.492
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- Publication type:
- Article
Congenital dyserythropoietic anaemias: new acquisitions.
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- Blood Transfusion (17232007), 2011, v. 9, n. 3, p. 278, doi. 10.2450/2010.0085-10
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- Publication type:
- Article
Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias.
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- International Journal of Laboratory Hematology, 2024, v. 46, n. 4, p. 595, doi. 10.1111/ijlh.14307
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- Publication type:
- Article
Diagnosis and molecular characterization of a novel α<sup>0</sup>-thalassemia deletion (- Kozani) found in a Greek child with unexplained microcytic hypochromic anemia.
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- International Journal of Laboratory Hematology, 2017, v. 39, n. 5, p. e124, doi. 10.1111/ijlh.12690
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- Publication type:
- Article
ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.
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- International Journal of Laboratory Hematology, 2015, v. 37, n. 3, p. 304, doi. 10.1111/ijlh.12335
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- Publication type:
- Article
Rapid detection of neonatal sepsis using polymerase chain reaction.
- Published in:
- 1997
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- Publication type:
- journal article
An Integrated Care Approach to Improve Well-Being in Breast Cancer Patients.
- Published in:
- Current Oncology Reports, 2024, v. 26, n. 4, p. 346, doi. 10.1007/s11912-024-01500-1
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- Publication type:
- Article
GENETIC CHARACTERIZATION OF AÂ COHORT OF PATIENTS AFFECTED BY SCHIZOPHRENIA. THE ROLE FOR RARE STRUCTURAL VARIANTS IN MODULATING TREATMENT RESISTANT ENDOPHENOTYPES: PRELIMINARY DATA.
- Published in:
- Schizophrenia Bulletin, 2020, v. 46, p. S201, doi. 10.1093/schbul/sbaa030.482
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- Publication type:
- Article
ALPL Genotypes in Patients With Atypical Femur Fractures or Other Biochemical and Clinical Signs of Hypophosphatasia.
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- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 5, p. e2087, doi. 10.1210/clinem/dgab914
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- Publication type:
- Article
The Rationale for Using Neridronate in Musculoskeletal Disorders: From Metabolic Bone Diseases to Musculoskeletal Pain.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 13, p. 6921, doi. 10.3390/ijms23136921
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- Publication type:
- Article
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 3, p. 1304, doi. 10.3390/ijms23031304
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- Publication type:
- Article
Role of the Endocannabinoid/Endovanilloid System in the Modulation of Osteoclast Activity in Paget's Disease of Bone.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 18, p. 10158, doi. 10.3390/ijms221810158
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- Publication type:
- Article
Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 10, p. 5372, doi. 10.3390/ijms22105372
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- Publication type:
- Article
The Rationale for the Intra-Articular Administration of Clodronate in Osteoarthritis.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 5, p. 2693, doi. 10.3390/ijms22052693
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- Publication type:
- Article
RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 15, p. 5577, doi. 10.3390/ijms21155577
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- Publication type:
- Article
FGFR1 is a potential therapeutic target in neuroblastoma.
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- Cancer Cell International, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12935-022-02587-x
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- Publication type:
- Article
Transient osteoporosis of the hip and subclinical hypothyroidism: an unusual dangerous duet? Case report and pathogenetic hypothesis.
- Published in:
- 2020
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- Publication type:
- journal article
Neonatal hyperbilirubinemia and Gilbert's syndrome.
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- Journal of Perinatal Medicine, 2002, v. 30, n. 2, p. 166
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- Publication type:
- Article
Renal vein thrombosis in a newborn with prothrombotic genetic risk factors.
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- Journal of Perinatal Medicine, 2001, v. 29, n. 2, p. 163
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- Publication type:
- Article
Safety of intra-articular hip injection of hyaluronic acid products by ultrasound guidance: an open study from ANTIAGE register.
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- European Review for Medical & Pharmacological Sciences, 2013, v. 17, n. 13, p. 1752
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- Publication type:
- Article
RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism.
- Published in:
- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 1, p. 1, doi. 10.1002/mgg3.1561
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- Publication type:
- Article
Genetic counseling during COVID‐19 pandemic: Tuscany experience.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1433
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- Publication type:
- Article
Label-free liquid biopsy through the identification of tumor cells by machine learning-powered tomographic phase imaging flow cytometry.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-32110-9
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- Publication type:
- Article
Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiency.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-31571-2
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- Publication type:
- Article
MDM2 SNP309 and p53 Arg72Pro in cutaneous melanoma: association between SNP309 GG genotype and tumor Breslow thickness.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 8, p. 518, doi. 10.1038/jhg.2010.62
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- Publication type:
- Article
Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anaemia (CDA II).
- Published in:
- Bone Marrow Transplantation, 2001, v. 27, n. 2, p. 213, doi. 10.1038/sj.bmt.1702764
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- Publication type:
- Article
Osteosarcopenia and type 2 diabetes mellitus in post-menopausal women: a case-control study.
- Published in:
- 2022
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- Publication type:
- Case Study
How to improve the outcomes of surgically treated proximal humeral osteoporotic fractures? A narrative review.
- Published in:
- Orthopedic Reviews, 2020, v. 12, n. 2, p. 54, doi. 10.4081/or.2020.8529
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- Publication type:
- Article
Genetic predictors of response to treatment of chronic hepatitis C virus infection in patients from southern Italy.
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- Italian Journal of Medicine, 2015, v. 9, n. 1, p. 61, doi. 10.4081/itjm.2014.443
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- Publication type:
- Article
SOCS3 and IRS-1 gene expression differs between genotype 1 and genotype 2 hepatitis C virus-infected HepG2 cells.
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- Clinical Chemistry & Laboratory Medicine, 2009, v. 47, n. 10, p. 1217, doi. 10.1515/CCLM.2009.280
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- Publication type:
- Article
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 5, p. 1348, doi. 10.1002/ajmg.a.38146
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- Publication type:
- Article
Are dietary supplements and nutraceuticals effective for musculoskeletal health and cognitive function? A scoping review.
- Published in:
- Journal of Nutrition, Health & Aging, 2017, v. 21, n. 5, p. 527, doi. 10.1007/s12603-016-0823-x
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- Publication type:
- Article
Transforming Growth Factor-β1 Gene Polymorphism, Bone Turnover, and Bone Mass in Italian Postmenopausal Women.
- Published in:
- Journal of Bone & Mineral Research, 2000, v. 15, n. 4, p. 634, doi. 10.1359/jbmr.2000.15.4.634
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- Publication type:
- Article
The use of next‐generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper*.
- Published in:
- British Journal of Haematology, 2022, v. 198, n. 3, p. 459, doi. 10.1111/bjh.18191
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- Publication type:
- Article
Advances in understanding the pathogenesis of red cell membrane disorders.
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- British Journal of Haematology, 2019, v. 187, n. 1, p. 13, doi. 10.1111/bjh.16126
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- Publication type:
- Article
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.
- Published in:
- Nature Genetics, 2012, v. 44, n. 10, p. 1126, doi. 10.1038/ng.2387
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- Publication type:
- Article