AGUENNOUZ, M'hammed
 Distribuzione geografica
Continente #
EU - Europa 445
NA - Nord America 95
AS - Asia 53
SA - Sud America 5
AF - Africa 3
Totale 601
Nazione #
IT - Italia 264
US - Stati Uniti d'America 94
IE - Irlanda 76
FR - Francia 27
VN - Vietnam 27
PL - Polonia 18
IN - India 15
CZ - Repubblica Ceca 10
RU - Federazione Russa 10
GB - Regno Unito 8
UA - Ucraina 8
NL - Olanda 7
DE - Germania 4
HR - Croazia 4
RO - Romania 4
CO - Colombia 3
CN - Cina 2
JP - Giappone 2
NG - Nigeria 2
SE - Svezia 2
BE - Belgio 1
BR - Brasile 1
CA - Canada 1
EG - Egitto 1
FI - Finlandia 1
HK - Hong Kong 1
ID - Indonesia 1
PH - Filippine 1
SA - Arabia Saudita 1
SG - Singapore 1
SK - Slovacchia (Repubblica Slovacca) 1
TR - Turchia 1
TW - Taiwan 1
UY - Uruguay 1
Totale 601
Città #
Messina 143
Dublin 76
Columbus 27
Dong Ket 26
Rome 18
Warsaw 18
Houston 12
Boardman 8
Piazza Armerina 7
Ashburn 6
Caltagirone 5
Paris 4
Castelfranco Veneto 3
Catania 3
Chicago 3
Kolkata 3
London 3
Padova 3
Palermo 3
Parsippany 3
Amsterdam 2
Bogotá 2
Bucharest 2
Council Bluffs 2
Craiova 2
Dallas 2
Dunfermline 2
Fleming Island 2
Floresville 2
Gatchina 2
Hamirpur 2
Hyderabad 2
Milan 2
Mountain View 2
Mumbai 2
Napa 2
Norwalk 2
Nuremberg 2
Pavia 2
Perm 2
Stockholm 2
The Villages 2
Voronezh 2
Aartselaar 1
Acireale 1
Alba 1
Bari 1
Bengaluru 1
Benin City 1
Berlin 1
Bratislava 1
Brescia 1
Cairo 1
Carterton 1
Cervignano del Friuli 1
Cesano Maderno 1
Chiyoda-ku 1
Comacchio 1
Daxini Society 1
Empoli 1
Falls Church 1
Florence 1
Gurgaon 1
Ha Kwai Chung 1
Hanoi 1
Hebei 1
Iikura 1
Konya 1
Lagos 1
Lahug 1
Lappeenranta 1
Livorno 1
Los Angeles 1
Medellín 1
Merselo 1
Mineo 1
Misterbianco 1
Montevideo 1
Montreal 1
Moscow 1
Naples 1
New York 1
Newark 1
Nizhniy Novgorod 1
Pekanbaru 1
Riyadh 1
Salete 1
Schio 1
Scordia 1
Siena 1
Sortino 1
Spokane 1
Tiruchirappalli 1
Trento 1
Turin 1
Ujjain 1
Venezia 1
Vizzini 1
Wentzville 1
Yekaterinburg 1
Totale 477
Nome #
Advances in Treatment of ATTRv Amyloidosis: State of the Art and Future Prospects, file de3e52b3-bb8e-762d-e053-3705fe0a30e0 78
MiRNA expression profiling regulates necroptotic cell death in hepatocellular carcinoma, file de3e52b1-f530-762d-e053-3705fe0a30e0 76
PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementation., file de3e52b2-e474-762d-e053-3705fe0a30e0 56
null, file de3e52b2-1d60-762d-e053-3705fe0a30e0 27
Idrocefalo normoteso idiopatico (iNPH): nostra esperienza preliminare., file de3e52b3-9244-762d-e053-3705fe0a30e0 26
Hippo signaling pathway is altered in Duchenne muscular dystrophy, file de3e52b1-ac65-762d-e053-3705fe0a30e0 22
Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination, file de3e52b1-c140-762d-e053-3705fe0a30e0 22
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment, file de3e52b1-f419-762d-e053-3705fe0a30e0 22
Prognostic value of HMGB1 and oxidative stress markers in multiple trauma patients: A single-centre prospective study, file de3e52b3-3017-762d-e053-3705fe0a30e0 22
MiRNA expression profiling regulates necroptotic cell death in hepatocellular carcinoma, file de3e52b4-8f4a-762d-e053-3705fe0a30e0 22
Prognostic value of HMGB1 and oxidative stress markers in multiple trauma patients: A single-centre prospective study, file de3e52b1-469a-762d-e053-3705fe0a30e0 20
miRNA regulation of Sirtuin-1 expression in human astrocytoma, file de3e52b3-5d6b-762d-e053-3705fe0a30e0 20
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination, file de3e52b4-90b0-762d-e053-3705fe0a30e0 15
Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological Diseases, file 0a80fe5c-0760-4a6c-8332-9c51228890ed 13
The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders., file de3e52b2-082b-762d-e053-3705fe0a30e0 11
A Phase 1/2 Study of Flavocoxid, an Oral NF-κB Inhibitor, in Duchenne Muscular Dystrophy, file de3e52b3-980e-762d-e053-3705fe0a30e0 10
Matrix Metalloproteinase 9 and Transglutaminase 2 Expression at the Ocular Surface in Patients with Different Forms of Dry Eye Disease, file de3e52b3-2f29-762d-e053-3705fe0a30e0 8
Circulating miRNAs expression as potential biomarkers of mild traumatic brain injury., file de3e52b2-9868-762d-e053-3705fe0a30e0 7
Charcot-Marie-Tooth disease: experience from a large Italian tertiary neuromuscular center, file de3e52b2-ef82-762d-e053-3705fe0a30e0 7
Modulation of neuronal nitric oxide synthase and apoptosis by the isoflavone genistein in Mdx mice, file de3e52af-7788-762d-e053-3705fe0a30e0 6
ANT1 is reduced in sporadic inclusion body myositis., file de3e52af-be7b-762d-e053-3705fe0a30e0 6
SIRT1 and SIRT2 Expression correlates with advanced disease and bone lesions in Multiple Myeloma, file de3e52b3-2acf-762d-e053-3705fe0a30e0 5
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects, file de3e52b4-8a2d-762d-e053-3705fe0a30e0 5
MiRNA expression profiling in human gliomas: upregulated miR-363 increases cell survival and proliferation, file de3e52b4-b2a7-762d-e053-3705fe0a30e0 5
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders, file 271dbdf4-a4cc-4527-8b40-631f4c41f140 4
Methylome Analysis in Nonfunctioning and GH-Secreting Pituitary Adenomas, file 7fde4649-266e-46b2-9dc5-c0f76cf7292d 4
Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathies, file de3e52ae-b142-762d-e053-3705fe0a30e0 4
Specific matrix metalloproteinase expression in focal myositis: an immunopathological study, file de3e52ae-b70b-762d-e053-3705fe0a30e0 4
null, file de3e52b1-fa3e-762d-e053-3705fe0a30e0 4
Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients., file de3e52ae-acd6-762d-e053-3705fe0a30e0 3
Flavocoxid counteracts muscle necrosis and improves functional properties in mdx mice: a comparison study with methylprednisolone, file de3e52ae-bf76-762d-e053-3705fe0a30e0 3
Reliability of clinical outcome measures in Charcot-Marie-Tooth disease, file de3e52ae-ccbd-762d-e053-3705fe0a30e0 3
Matrix Metalloproteinase 9 and Transglutaminase 2 Expression at the Ocular Surface in Patients with Different Forms of Dry Eye Disease, file de3e52ae-ec46-762d-e053-3705fe0a30e0 3
MicroRNAs expression in pituitary tumors: differences related to functional status, pathological features, and clinical behavior, file de3e52b2-217b-762d-e053-3705fe0a30e0 3
null, file de3e52b2-ef86-762d-e053-3705fe0a30e0 3
Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development, file 852fcc18-3b33-4f80-9eb1-beaa0a2f1baf 2
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease, file c8a2e712-91ba-471f-aa71-d43c17e1697f 2
Type I hyperprolinemia and proline dehydrogenase (PRODH) mutations in four Italian children with epilepsy and mental retardation., file de3e52ae-a42b-762d-e053-3705fe0a30e0 2
Immunolocalization and activation of nuclear factor-kappa B in the sciatic nerves of rats with experimental autoimmune neuritis, file de3e52ae-bfc7-762d-e053-3705fe0a30e0 2
Limb-girdle myasthenia: clinical, electrophysiological and morphological features in familial and autoimmune cases, file de3e52ae-cb4b-762d-e053-3705fe0a30e0 2
RAGE-NF-kappa B pathway activation in response to oxidative stress in facioscapulohumeral muscular dystrophy, file de3e52ae-ccb4-762d-e053-3705fe0a30e0 2
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial, file de3e52ae-cebb-762d-e053-3705fe0a30e0 2
Telomere Length Modulation in Human Astroglial Brain Tumors, file de3e52ae-f2fd-762d-e053-3705fe0a30e0 2
Analysis of lipid profile in lipid storage myopathy, file de3e52b0-18bb-762d-e053-3705fe0a30e0 2
MicroRNA signatures predict dysregulated Vitamin D receptor and calcium pathways status in Limb Girdle muscle dystrophies (LGMD) 2A/2B., file de3e52b0-69af-762d-e053-3705fe0a30e0 2
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination, file de3e52b2-1306-762d-e053-3705fe0a30e0 2
Role of Erythropoietin in Cerebral Glioma: An Innovative Target in Neuro-Oncology, file de3e52b2-6332-762d-e053-3705fe0a30e0 2
Autoimmunity to heterogeneous nuclear ribonucleoprotein A1 in psoriatic patients and correlation with disease severity, file de3e52b2-c823-762d-e053-3705fe0a30e0 2
Nuclear factor-κB activation and differential expression of survivin and Bcl-2 in human grade 2-4 astrocytomas, file de3e52b3-03d7-762d-e053-3705fe0a30e0 2
Circulating microRNAs Profile in Patients With Transthyretin Variant Amyloidosis, file de3e52b3-129c-762d-e053-3705fe0a30e0 2
SIRT2 and SIRT3 expression correlates with redox imbalance and advanced clinical stage in patients with multiple myeloma, file de3e52b5-11f6-762d-e053-3705fe0a30e0 2
(+)-Lipoic Acid Reduces Lipotoxicity and Regulates Mitochondrial Homeostasis and Energy Balance in an In Vitro Model of Liver Steatosis, file 6d892a7b-ef47-4022-844d-a2c1e923624e 1
A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): the study protocol, file de3e52ae-ad6c-762d-e053-3705fe0a30e0 1
Fatal exacerbation of peripheral neuropathy during lamivudine therapy: evidence for iatrogenic mitochondrial damage, file de3e52ae-b986-762d-e053-3705fe0a30e0 1
VEGF overexpression via adeno-associated virus gene transfer promotes skeletal muscle regeneration and enhances muscle function in mdx mice, file de3e52ae-bed6-762d-e053-3705fe0a30e0 1
Calpain 3 deficiency in Quail Eater's disease, file de3e52ae-c669-762d-e053-3705fe0a30e0 1
Regulation of interleukin-8 gene at a distinct site of its promoter by C/EBP homologous protein in prostaglandin E2-treated human T cells, file de3e52ae-c8f2-762d-e053-3705fe0a30e0 1
Telomere shortening is associated to TRF1 and PARP1 overexpression in Duchenne muscular dystrophy, file de3e52ae-c903-762d-e053-3705fe0a30e0 1
null, file de3e52ae-dfea-762d-e053-3705fe0a30e0 1
null, file de3e52ae-fe21-762d-e053-3705fe0a30e0 1
MDR-1 gene polymorphisms G2677T and C3435T in a case of Hodgkin's variant of Richter's syndrome, file de3e52b0-3cbc-762d-e053-3705fe0a30e0 1
null, file de3e52b0-6649-762d-e053-3705fe0a30e0 1
Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiency, file de3e52b0-82e0-762d-e053-3705fe0a30e0 1
Telomere instability in papillary bladder urothelial carcinomas: Comparison with grading and risk of recurrence, file de3e52b0-b637-762d-e053-3705fe0a30e0 1
null, file de3e52b1-6174-762d-e053-3705fe0a30e0 1
null, file de3e52b1-c2dc-762d-e053-3705fe0a30e0 1
NLRP3 inflammasome CSF expression and neuropsychological changes in idiopathic normal pressure hydrocephalus, file de3e52b1-f48f-762d-e053-3705fe0a30e0 1
MiRNA expression profiling in human gliomas: upregulated miR-363 increases cell survival and proliferation, file de3e52b2-028e-762d-e053-3705fe0a30e0 1
A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration, file de3e52b2-3012-762d-e053-3705fe0a30e0 1
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants, file de3e52b4-7a3d-762d-e053-3705fe0a30e0 1
Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological Diseases, file de3e52b4-7a43-762d-e053-3705fe0a30e0 1
Rare among rare: Phenotypes of uncommon CMT genotypes, file de3e52b5-7f5b-762d-e053-3705fe0a30e0 1
Totale 602
Categoria #
all - tutte 1.814
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 1.814


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202047 0 0 0 0 0 0 1 0 11 11 9 15
2020/2021162 13 4 8 10 3 1 8 9 28 49 1 28
2021/202273 3 0 4 4 2 7 0 8 7 8 24 6
2022/2023140 3 7 2 7 11 7 11 9 59 2 16 6
2023/2024165 6 15 18 18 5 11 22 3 15 7 45 0
Totale 602