| Nome |
# |
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Wolfram Syndrome 1: From Genetics to Therapy, file 69b6142e-6415-41f9-afc6-5093fe719982
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131
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An Atypical Case of Late-Onset Wolfram Syndrome 1 without Diabetes Insipidus, file c884136c-92bc-4177-aa0f-bfc7da2ed426
|
46
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HER2 status in premalignant, early, and advanced neoplastic lesions of the stomach, file de3e52af-8b37-762d-e053-3705fe0a30e0
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24
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Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease, file de3e52b1-ca3e-762d-e053-3705fe0a30e0
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23
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Morphological and cellular features of innate immune reaction in helicobacter pylori gastritis: A brief review, file de3e52b0-0cbe-762d-e053-3705fe0a30e0
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20
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Phagocytosis (cannibalism) of apoptotic neutrophils by tumor cells in gastric micropapillary carcinomas, file de3e52af-8b3b-762d-e053-3705fe0a30e0
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19
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Immunohistochemical expression of autophagy-related proteins in advanced tubular gastric adenocarcinomas and its implications, file de3e52b2-1638-762d-e053-3705fe0a30e0
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17
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Prevalence of deafness-associated connexin-26 (GJB2) and connexin-30 (GJB6) pathogenic alleles in a large patient cohort from Eastern Sicily, file de3e52af-29a7-762d-e053-3705fe0a30e0
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15
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Tumor-Associated Neutrophils (TANs) in Gastric Carcinomas: Clinicopathological and Prognostic Implications, file de3e52b1-c7e1-762d-e053-3705fe0a30e0
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15
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Evolutionarily-related helicobacter pylori genotypes and gastric intraepithelial neoplasia in a high-risk area of northern Italy, file de3e52b2-ca59-762d-e053-3705fe0a30e0
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13
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Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1, file a9355e8e-0329-4902-9041-53c142d46c3d
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11
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Individuato il terzo caso di ipoacusia bilaterale del gene GJB2 dovuto alla mutazione M163V in una popolazione siciliana., file de3e52ae-cba2-762d-e053-3705fe0a30e0
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8
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Early identification of cardiovascular involvement in patients with β-thalassemia major, file de3e52ae-f774-762d-e053-3705fe0a30e0
|
8
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Endocrinopathies, metabolic disorders, and iron overload in major and intermedia thalassemia: Serum ferritin as diagnostic and predictive marker associated with liver and cardiac T2* MRI assessment, file de3e52b0-298d-762d-e053-3705fe0a30e0
|
8
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|
Prevalence of deafness-associated connexin-26 (GJB2) and connexin-30 (GJB6) pathogenic alleles in a large patient cohort from Eastern Sicily, file de3e52b3-9cca-762d-e053-3705fe0a30e0
|
8
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null, file de3e52ae-a0ad-762d-e053-3705fe0a30e0
|
7
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null, file de3e52ae-a0b7-762d-e053-3705fe0a30e0
|
7
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|
null, file de3e52b0-3284-762d-e053-3705fe0a30e0
|
7
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Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia, file de3e52b0-3286-762d-e053-3705fe0a30e0
|
7
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A novel mutation of the δ-Globin Gene in an Asymptomatic 30-Year-Old Female, file de3e52b1-ca02-762d-e053-3705fe0a30e0
|
7
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Wolfram syndrome 1 in the Italian population: genotype–phenotype correlations, file de3e52b2-acf8-762d-e053-3705fe0a30e0
|
7
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Gene-environment interaction in childhood asthma., file de3e52af-076b-762d-e053-3705fe0a30e0
|
6
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The era of comparable life expectancy between thalassaemia major and intermedia: Is it time to revisit the major-intermedia dichotomy?, file de3e52b2-abb7-762d-e053-3705fe0a30e0
|
6
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Thalassaemia major and infectious risk: High Mobility Group Box-1 represents a novel diagnostic and prognostic biomarker, file de3e52b3-4804-762d-e053-3705fe0a30e0
|
6
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What syndrome is this? Kabuki make-up syndrome (Niikawa-Kuroki syndrome), file de3e52ae-ca55-762d-e053-3705fe0a30e0
|
5
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Wolfram syndrome and WFS1 gene, file de3e52ae-e1bd-762d-e053-3705fe0a30e0
|
5
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Iron overload and malignancies in patients with haemoglobinopathies: A single center experience, file de3e52b2-dbc9-762d-e053-3705fe0a30e0
|
5
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A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1, file de3e52ae-cbb6-762d-e053-3705fe0a30e0
|
4
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Due casi di carcinoma tiroideo in pazienti affetti da talassemia, file de3e52ae-e5c7-762d-e053-3705fe0a30e0
|
4
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The era of comparable life expectancy between thalassaemia major and intermedia: Is it time to revisit the major-intermedia dichotomy?, file de3e52b3-74a1-762d-e053-3705fe0a30e0
|
4
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Deferiprone versus deferoxamine in thalassemia intermedia: Results from a 5-year long-term Italian multicenter randomized clinical trial, file de3e52b4-8122-762d-e053-3705fe0a30e0
|
4
|
|
Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies, file de3e52ae-b398-762d-e053-3705fe0a30e0
|
3
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Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease., file de3e52ae-d520-762d-e053-3705fe0a30e0
|
3
|
|
Foveolar cells
phagocytose apoptotic neutrophils in chronic active Helicobacter pylori
gastritis, file de3e52ae-de3a-762d-e053-3705fe0a30e0
|
3
|
|
Phenotypical and genotypical expression of Wolfram syndrome in 12 patients from a
Sicilian district where this syndrome might not be so infrequent as generally
expected., file de3e52ae-f037-762d-e053-3705fe0a30e0
|
3
|
|
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders, file de3e52b0-8c26-762d-e053-3705fe0a30e0
|
3
|
|
Gastric adenomas: relationship between clinicopathological findings, Helicobacter pylori infection, APC mutations and COX-2 expression, file de3e52ae-bbfb-762d-e053-3705fe0a30e0
|
2
|
|
CEP290 Mutations Are Frequently Identified in the Oculo-Renal Form of Joubert Syndrome Related Disorders, file de3e52ae-ccb8-762d-e053-3705fe0a30e0
|
2
|
|
Genotoxicity biomarkers in thalassaemic patients, file de3e52ae-cd01-762d-e053-3705fe0a30e0
|
2
|
|
TLR2 and TLR4 gene polymorphisms and atopic dermatitis in Italian children: a multicenter study, file de3e52ae-ce94-762d-e053-3705fe0a30e0
|
2
|
|
Gene-environment interaction in childhood asthma, file de3e52ae-e145-762d-e053-3705fe0a30e0
|
2
|
|
Morphological evidence of neutrophil-tumor cell phagocytosis (cannibalism) in human gastric adenocarcinomas, file de3e52b0-7baf-762d-e053-3705fe0a30e0
|
2
|
|
Eosinophil-Specific Granules in Tumor Cell Cytoplasm: Unusual Ultrastructural Findings in a Case of Diffuse-Type Gastric Carcinoma, file de3e52b0-8574-762d-e053-3705fe0a30e0
|
2
|
|
Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome, file de3e52b0-9700-762d-e053-3705fe0a30e0
|
2
|
|
M1 Polarized Tumor-Associated Macrophages (TAMs) as Promising Prognostic Signature in Stage I–II Gastric Adenocarcinomas, file de3e52b5-0505-762d-e053-3705fe0a30e0
|
2
|
|
Wolfram syndrome 1 in the Italian population: genotype–phenotype correlations, file fe371a58-9326-4665-9f6e-985ed1d44936
|
2
|
|
Eosinophil exocytosis in a poorly differentiated tubular gastric adenocarcinoma:case report., file 8cbd29b9-7b6a-49c5-a3fd-91c76408dfe9
|
1
|
|
Allergen immunotherapy, routes of
administration and cytokine networks:
an update, file de3e52ae-a08a-762d-e053-3705fe0a30e0
|
1
|
|
Investigation of the eotaxin gene -426C-->T, -384A-->G and 67G-->a single-nucleotide polymorphisms and atopic dermatitis in Italian children using family-based association methods., file de3e52ae-b25a-762d-e053-3705fe0a30e0
|
1
|
|
Report of a third family with Oliver syndrome, file de3e52ae-b381-762d-e053-3705fe0a30e0
|
1
|
|
MKS3/TMEM67 Mutations Are a Major Cause of COACH Syndrome, a Joubert Syndrome Related Disorder with Liver Involvement, file de3e52ae-c62f-762d-e053-3705fe0a30e0
|
1
|
|
The role of the incidence of genetic adnormalities on the onset and on the results of the surgical repair of varicocele, file de3e52ae-d86b-762d-e053-3705fe0a30e0
|
1
|
|
Identification of one novel causative mutation in exon 4 of WFS1 gene in two
Italian siblings with classical DIDMOAD syndrome phenotype., file de3e52ae-dca6-762d-e053-3705fe0a30e0
|
1
|
|
Serum IL-23 in asthmatic children., file de3e52ae-dcba-762d-e053-3705fe0a30e0
|
1
|
|
Serum IL-23 Strongly and Inversely Correlates with FEV(1) in Asthmatic Children, file de3e52ae-e13a-762d-e053-3705fe0a30e0
|
1
|
|
Mitochondrial DNA alterations in the progression of
gastric carcinomas: unexplored issues and future research needs., file de3e52af-0766-762d-e053-3705fe0a30e0
|
1
|
|
Wolfram syndrome 1 and Wolfram syndrome 2., file de3e52af-076a-762d-e053-3705fe0a30e0
|
1
|
|
Molecular analysis of beta-thalassaemia patients in a high incidence area of southern Italy., file de3e52b0-72be-762d-e053-3705fe0a30e0
|
1
|
|
Eosinophil-tumor cell interaction in advanced gastric carcinoma: An electron microscopic approach, file de3e52b0-906b-762d-e053-3705fe0a30e0
|
1
|
|
Diabetes in Wolfram syndrome: update of clinical and genetic aspects., file de3e52b3-322a-762d-e053-3705fe0a30e0
|
1
|
| Totale |
506 |