| Nome |
# |
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Case Report: Morphologic and Functional Characteristics of Intestinal Mucosa in a Child With Short Bowel Syndrome After Treatment With Teduglutide: Evidence in Favor of GLP-2 Analog Safety, file 1d7fb1c1-5822-4f33-9573-937e2db85d75
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739
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Mesenchymal stem cells in renal function recovery after acute kidney injury. Use of a differentiating agent in a rat model., file e1dcb332-8a09-7715-e053-1705fe0a6cc9
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242
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Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy, file e1dcb339-ea5f-7715-e053-1705fe0a6cc9
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136
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Liver as a Source for Thymidine Phosphorylase Replacement in Mitochondrial Neurogastrointestinal Encephalomyopathy, file e1dcb32c-5d0b-7715-e053-1705fe0a6cc9
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111
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Medullospheres from DAOY, UW228 and ONS-76 Cells: Increased Stem Cell Population and Proteomic Modifications., file e1dcb32d-4bed-7715-e053-1705fe0a6cc9
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100
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The empowerment of translational research: lessons from laminopathies., file e1dcb32d-1ff3-7715-e053-1705fe0a6cc9
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97
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Differentiation of mesenchymal stem cells derived from pancreatic islets and bone marrow into islet-like cell phenotype., file e1dcb32d-3dff-7715-e053-1705fe0a6cc9
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90
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XAV939-mediated ARTD activity inhibition in human MB cell lines, file e1dcb32d-bf82-7715-e053-1705fe0a6cc9
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87
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Response of human chondrocytes and mesenchymal stromal cells to a decellularized human dermis, file e1dcb333-4b81-7715-e053-1705fe0a6cc9
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87
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Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α., file e1dcb334-b0bd-7715-e053-1705fe0a6cc9
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82
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Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy, file e1dcb335-6972-7715-e053-1705fe0a6cc9
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76
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Kidney biopsy findings in a critically ill COVID-19 patient with dialysis-dependent. acute kidney injury: a case against “SARS-CoV-2 nephropathy, file e1dcb335-c683-7715-e053-1705fe0a6cc9
|
67
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Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function, file e1dcb330-6440-7715-e053-1705fe0a6cc9
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64
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A Rare Case of Systemic AL Amyloidosis with Muscle Involvement: A Misleading Diagnosis, file e1dcb331-f5d7-7715-e053-1705fe0a6cc9
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63
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Different renal phenotypes in related adult males with Fabry disease with the same classic genotype, file e1dcb330-8292-7715-e053-1705fe0a6cc9
|
56
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Sub-Populations of Dermal Skin Fibroblasts Secrete Distinct Extracellular Matrix: Implications for Using Skin Substitutes in the Clinic, file e1dcb330-2f6f-7715-e053-1705fe0a6cc9
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44
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X-linked duchenne-type muscular dystrophy in Jack Russell Terrier associated with a partial deletion of the canine DMD gene, file e1dcb335-f995-7715-e053-1705fe0a6cc9
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44
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An Abnormal Host/Microbiomes Signature of Plasma-Derived Extracellular Vesicles Is Associated to Polycythemia Vera, file e1dcb338-ff8c-7715-e053-1705fe0a6cc9
|
36
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Cardiac Functional and Structural Abnormalities in a Mouse Model of CDKL5 Deficiency Disorder, file d22f8701-e733-4042-ab0f-eacae4e8de47
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31
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Androgen-dependent impairment of myogenesis in spinal and bulbar muscular atrophy, file e1dcb32d-46a2-7715-e053-1705fe0a6cc9
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31
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LGMD D2 TNPO3-Related: From Clinical Spectrum to Pathogenetic Mechanism., file e1dcb339-906a-7715-e053-1705fe0a6cc9
|
30
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Anatomical Laser Microdissection of the Ileum Reveals mtDNA Depletion Recovery in A Mitochondrial Neuro-Gastrointestinal Encephalomyopathy (MNGIE) Patient Receiving Liver Transplant, file 4ba31a0b-c69b-4368-a4bd-1a4a3de402d7
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27
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Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function, file e1dcb335-373f-7715-e053-1705fe0a6cc9
|
24
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Electrospun Poly(L-lactide-co-ε-caprolactone) Scaffold Potentiates C2C12 Myoblast Bioactivity and Acts as a Stimulus for Cell Commitment in Skeletal Muscle Myogenesis, file e068f035-1dff-4e55-9245-cd24571b6738
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23
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Oxalate Nephropathy Caused by Excessive Vitamin C Administration in 2 Patients With COVID-19, file e1dcb336-f075-7715-e053-1705fe0a6cc9
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21
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Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy, file 668c9708-4cc7-4fa6-99b2-459818c1040d
|
17
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Case Report: Morphologic and Functional Characteristics of Intestinal Mucosa in a Child With Short Bowel Syndrome After Treatment With Teduglutide: Evidence in Favor of GLP-2 Analog Safety, file d0ca7ea6-8db8-4ca5-a2b8-5be2f3535b60
|
12
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Skeletal muscle pathology in MNGIE patients: blood vessels depletion, file e1dcb335-3059-7715-e053-1705fe0a6cc9
|
11
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Sickle Cell Trait and SARS-CoV-2-Induced Rhabdomyolysis: A Case Report, file e1dcb339-c9a7-7715-e053-1705fe0a6cc9
|
11
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Pulmonary fibrosis in a dog as a sequela of infection with Severe Acute Respiratory Syndrome Coronavirus 2? A case report, file 018f7804-33a5-4177-8ed5-71433d609f58
|
9
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Brain ischemic injury in COVID-19-infected patients: a series of 10 post-mortem cases, file ad3302bf-5703-4a6b-bc2d-6059c96412d1
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9
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CD99 suppresses osteosarcoma cell migration through inhibition of ROCK2 activity., file e1dcb32c-1a06-7715-e053-1705fe0a6cc9
|
8
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Kidney biopsy findings in a critically ill COVID-19 patient with dialysis-dependent. acute kidney injury: a case against “SARS-CoV-2 nephropathy, file e1dcb335-c684-7715-e053-1705fe0a6cc9
|
8
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Renal thrombotic microangiopathy in concurrent COVID-19 vaccination and infection, file e1dcb338-dfa3-7715-e053-1705fe0a6cc9
|
8
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Morphological study of TNPO3 and SRSF1 interaction during myogenesis by combining confocal, structured illumination and electron microscopy analysis, file e1dcb336-6a8c-7715-e053-1705fe0a6cc9
|
7
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Small heat-shock protein HSPB3 promotes myogenesis by regulating the lamin B receptor, file e1dcb339-10c4-7715-e053-1705fe0a6cc9
|
7
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Glucocorticoid receptor antagonization propels endogenous cardiomyocyte proliferation and cardiac regeneration, file 28b0f804-1dc7-400d-b908-59593837a067
|
5
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Dilated intercellular spaces as a marker of oesophageal damage: Comparative results in gastro-oesophageal reflux disease with or without bile reflux, file e1dcb336-6ca5-7715-e053-1705fe0a6cc9
|
5
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Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy, file e1dcb338-a379-7715-e053-1705fe0a6cc9
|
5
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Brain ischemic injury in COVID-19-infected patients: a series of 10 post-mortem cases, file 02694ae7-56a1-4b96-a3ad-0a188104e293
|
4
|
|
Oxalate Nephropathy Caused by Excessive Vitamin C Administration in 2 Patients With COVID-19, file 92af6b88-baa5-43ef-805c-492d47545f55
|
4
|
|
COVID-19 and the Brain: The Neuropathological Italian Experience on 33 Adult Autopsies, file a7371dca-2065-4637-b327-9310629226a4
|
4
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|
An Abnormal Host/Microbiomes Signature of Plasma-Derived Extracellular Vesicles Is Associated to Polycythemia Vera, file 5e9c457d-6ff2-48a0-a0fe-49cdcbee910f
|
3
|
|
Proteomic analysis of extracellular vesicles from medullospheres reveals a role for iron in the cancer progression of medulloblastoma, file e1dcb32c-c9a9-7715-e053-1705fe0a6cc9
|
3
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Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure, file e1dcb32d-beb4-7715-e053-1705fe0a6cc9
|
3
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|
ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy., file e1dcb32d-f99b-7715-e053-1705fe0a6cc9
|
3
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|
Kidney biopsy findings in a critically ill COVID-19 patient with dialysis-dependent. acute kidney injury: a case against “SARS-CoV-2 nephropathy, file e1dcb335-5066-7715-e053-1705fe0a6cc9
|
3
|
|
Brain ischemic injury in COVID-19-infected patients: a series of 10 post-mortem cases, file e1dcb336-66fb-7715-e053-1705fe0a6cc9
|
3
|
|
Expanding the Clinical Spectrum of UBTF-Related Neurodevelopmental Disorder, file 87314fa3-828f-4397-92fe-45019f1fdcb8
|
2
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|
Decellularized human dermal matrix produced by a skin bank: A new treatment for abdominal wall defects, file e1dcb330-5fdf-7715-e053-1705fe0a6cc9
|
2
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|
Functional expression of calcium-permeable canonical transient receptor potential 4-containing channels promotes migration of medulloblastoma cells, file e1dcb330-643f-7715-e053-1705fe0a6cc9
|
2
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|
A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy, file e1dcb330-83a3-7715-e053-1705fe0a6cc9
|
2
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Minimal change disease during lithium therapy: case report, file e1dcb333-7973-7715-e053-1705fe0a6cc9
|
2
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Update on polyglucosan storage diseases, file e1dcb333-9e7f-7715-e053-1705fe0a6cc9
|
2
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|
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy, file e1dcb335-6974-7715-e053-1705fe0a6cc9
|
2
|
|
Cardiac Functional and Structural Abnormalities in a Mouse Model of CDKL5 Deficiency Disorder, file 9ca3ff53-4e7f-418e-a266-5734020a12a9
|
1
|
|
Fabry Disease Nephropathy: Histological Changes With Nonclassical Mutations and Genetic Variants of Unknown Significance, file d6546bbe-ffa9-40f4-8abc-0ccc91a97f9f
|
1
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|
Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations., file e1dcb32d-bf83-7715-e053-1705fe0a6cc9
|
1
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|
null, file e1dcb32d-fed8-7715-e053-1705fe0a6cc9
|
1
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null, file e1dcb32e-00b6-7715-e053-1705fe0a6cc9
|
1
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Building blocks of the GIPU, Italian Group of Ultrastructural Pathology, file e1dcb32f-9be4-7715-e053-1705fe0a6cc9
|
1
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Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy, file e1dcb32f-a5eb-7715-e053-1705fe0a6cc9
|
1
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Spontaneously occurring intramural coronary arteriosclerosis in regularly slaughtered veal calves and beef cattle: A screening study about prevalence and histopathological features, file e1dcb330-908e-7715-e053-1705fe0a6cc9
|
1
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Sleep and cardiovascular phenotype in middle-aged hypocretin-deficient narcoleptic mice, file e1dcb330-be9c-7715-e053-1705fe0a6cc9
|
1
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Transportin 3 (TNPO3) and related proteins in limb girdle muscle dystrophy D2 muscle biopsies: a morphological confocal microscopy study and pathogenetic hypothesis, file e1dcb335-40bc-7715-e053-1705fe0a6cc9
|
1
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|
Amyloid myopathy: an intriguing diagnosis., file e1dcb335-47d9-7715-e053-1705fe0a6cc9
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1
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The clinical and molecular spectrum of autosomal dominant limb-girdle muscular dystrophies focusing on ransportinopathy., file e1dcb335-5c39-7715-e053-1705fe0a6cc9
|
1
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A Pathogenic Galactosidase A Mutation Coexisting With an MYBPC3 Mutation in a Female Patient With Hypertrophic Cardiomyopathy, file e1dcb336-0989-7715-e053-1705fe0a6cc9
|
1
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|
Liver transplantation in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical long-term follow-up and pathogenic implications, file e1dcb336-1ef8-7715-e053-1705fe0a6cc9
|
1
|
|
Canine Mammary Carcinoma With Vacuolated Cytoplasm: Glycogen-Rich Carcinoma, a Histological Type Distinct From Lipid-Rich Carcinoma, file e1dcb336-875a-7715-e053-1705fe0a6cc9
|
1
|
|
Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy, file e1dcb338-f1d3-7715-e053-1705fe0a6cc9
|
1
|
|
Small heat-shock protein HSPB3 promotes myogenesis by regulating the lamin B receptor, file eb7a892e-a4b7-479a-b1b5-c8394dbffe90
|
1
|
| Totale |
2.591 |