IRIS
ROSSI, ALESSANDRO
 Distribuzione geografica
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Continente #
NA - Nord America 502
EU - Europa 337
AS - Asia 166
AF - Africa 26
SA - Sud America 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.034
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Nazione #
US - Stati Uniti d'America 492
IT - Italia 181
SG - Singapore 125
NL - Olanda 73
CN - Cina 30
CI - Costa d'Avorio 25
DE - Germania 22
IE - Irlanda 12
CA - Canada 10
FI - Finlandia 9
BG - Bulgaria 8
GB - Regno Unito 8
RU - Federazione Russa 6
IN - India 5
UA - Ucraina 5
FR - Francia 4
AR - Argentina 2
LV - Lettonia 2
SE - Svezia 2
BD - Bangladesh 1
CZ - Repubblica Ceca 1
EU - Europa 1
HU - Ungheria 1
IL - Israele 1
KG - Kirghizistan 1
LT - Lituania 1
MA - Marocco 1
MM - Myanmar 1
MO - Macao, regione amministrativa speciale della Cina 1
PL - Polonia 1
PT - Portogallo 1
VN - Vietnam 1
Totale 1.034
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Città #
Singapore 110
Santa Clara 76
Chandler 74
Amsterdam 53
Naples 47
Ashburn 43
Millbury 26
Lawrence 16
Napoli 11
Boston 10
Des Moines 9
Rome 8
Sofia 8
Groningen 7
Kronberg 6
Torre Annunziata 6
Wilmington 6
Frankfurt am Main 5
Jacksonville 5
Ottawa 5
Princeton 5
Afragola 4
Beijing 4
Caserta 4
Council Bluffs 4
Los Angeles 4
Milan 4
Redwood City 4
Andover 3
Boardman 3
Bologna 3
Buffalo 3
Lappeenranta 3
Marcianise 3
Nanjing 3
Portici 3
Pune 3
Volla 3
Avellino 2
Casavatore 2
Castignano 2
Columbus 2
Deiva Marina 2
Denver 2
Helsinki 2
Huizhou 2
Jiaxing 2
Kanniyākumāri 2
Modena 2
Montreal 2
Nanchang 2
Puerto Eldorado 2
Riga 2
San Mateo 2
Seattle 2
Toronto 2
Urbino 2
Washington 2
Woodbridge 2
Airola 1
Anacapri 1
Atripalda 1
Augusta 1
Bishkek 1
Brno 1
Budapest 1
Cambridge 1
Castellammare Di Stabia 1
Castellammare di Stabia 1
Cava De' Tirreni 1
Crawley 1
Dearborn 1
Dhaka 1
Ercolano 1
Fairfield 1
Falkenstein 1
Florence 1
Haifa 1
Hengyang 1
Houston 1
Islington 1
Kanata 1
Krefeld 1
Laojunmiao 1
Lisbon 1
London 1
Marano 1
Middletown 1
Monticelli 1
Morgan Hill 1
Moscow 1
Mugnano di Napoli 1
Nay Pyi Taw 1
New York 1
Newark 1
Norwalk 1
Paris 1
Piedimonte Matese 1
Positano 1
Rosmalen 1
Totale 677
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Nome #
Reduced bone mineral density in glycogen storage disease type III: Evidence for a possible connection between metabolic imbalance and bone homeostasis 59
Glycogen storage disease type Ia (GSDIa) but not Glycogen storage disease type Ib (GSDIb) is associated to an increased risk of metabolic syndrome: possible role of microsomal glucose 6-phosphate accumulation. 54
A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: A retrospective, single-center study and the generation of www.emergencyprotocol.net 52
Insulin-resistance in glycogen storage disease type Ia: linking carbohydrates and mitochondria? 48
An Overview of Hypoglycemia in Children Including a Comprehensive Practical Diagnostic Flowchart for Clinical Use 44
Plasma acylcarnitines and urine organic acids profiles provide evidence for possible mitochondrial dysfunction in glycogen storage disease type Ia 42
Imbalanced cortisol concentrations in glycogen storage disease type I: Evidence for a possible link between endocrine regulation and metabolic derangement 36
Bone metabolism in patients with type 1 neurofibromatosis: key role of sun exposure and physical activity 35
Biomarkers for gene therapy clinical trials of lysosomal storage disorders 33
Dynamic Methods for Childhood Hypoglycemia Phenotyping: A Narrative Review 32
Contribution of Genetic Test to Early Diagnosis of Methylenetetrahydrofolate Reductase (MTHFR) Deficiency: The Experience of a Reference Center in Southern Italy 31
Crohn disease-like enterocolitis remission after empagliflozin treatment in a child with glycogen storage disease type Ib: a case report 31
Galactosemia: Biochemistry, Molecular Genetics, Newborn Screening, and Treatment 30
Involvement of endocrine system in a patient affected by glycogen storage disease 1b: speculation on the role of autoimmunity 30
Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire 30
Mitochondrial reprogramming in peripheral blood mononuclear cells of patients with glycogen storage disease type Ia 29
Primrose syndrome: Characterization of the phenotype in 42 patients 29
Cervical spondylolisthesis in mucopolysaccharidosis type II 28
Bronchial isomerism in a Kabuki syndrome patient with a novel mutation in MLL2 gene 28
Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations. 26
Peritoneal tuberculosis mimicking carcinomatous ascites in a child living in a low prevalence country: a case report 25
Long-term monitoring for short/branched-chain acyl-CoA dehydrogenase deficiency: A single-center 4-year experience and open issues 24
Metabolic stroke-like events in a girl with pyruvate dehydrogenase complex deficiency caused by a novel de novo mutation in PDHA1 24
Glycogen storage disease type Ia: Current management options, burden and unmet needs 24
Long-term use of carglumic acid in methylmalonic aciduria, propionic aciduria and isovaleric aciduria in Italy: a qualitative survey 23
Liver-Directed Adeno-Associated Virus–Mediated Gene Therapy for Mucopolysaccharidosis Type VI 23
Multi-year enzyme expression in patients with mucopolysaccharidosis type VI after liver-directed gene therapy 21
Early diagnosis and treatment in a child with foodborne botulism 21
Clinical and biochemical footprints of inherited metabolic diseases. XIII. Respiratory manifestations 18
Rhabdomyolysis and coeliac disease: A causal or casual association? A case report and review of literature 18
A prospective study on continuous glucose monitoring in glycogen storage disease type Ia: towards glycemic targets 17
An asymptomatic father diagnosed with 3-methylcrotonyl-CoA carboxylase deficiency following his son newborn screening test 17
Severe hypercalcemia associated with hypophosphatemia in very premature infants: a case report 17
Nutritional management of glycogen storage disease type III: a case report and a critical appraisal of the literature 14
Towards values-based healthcare for inherited metabolic disorders: An overview of current practices for persons with liver glycogen storage disease and fatty acid oxidation disorders 12
Liver-directed gene-based therapies for inborn errors of metabolism 10
Gene therapies for mucopolysaccharidoses 9
Endocrine involvement in hepatic glycogen storage diseases: pathophysiology and implications for care 9
Empagliflozin for treating neutropenia and neutrophil dysfunction in 21 infants with glycogen storage disease 1b 8
Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop 8
Maleic acid is a biomarker for maleylacetoacetate isomerase deficiency; implications for newborn screening of tyrosinemia type 1 8
Endogenous Glucose Production in Patients With Glycogen Storage Disease Type Ia Estimated by Oral D-[6,6-2H2]-glucose 7
A specific serum lipid signature characterises patients with glycogen storage disease type Ia 5
Mapping challenges in the accessibility of treatment products for urea cycle disorders: A survey of European healthcare professionals 3
Continuous glucose monitoring metrics in people with liver glycogen storage disease and idiopathic ketotic hypoglycemia: A single-center, retrospective, observational study 3
Totale 1.095
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Categoria #
all - tutte 6.415
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 6.415
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202019 0 0 0 0 0 0 4 0 2 2 4 7
2020/202130 0 1 2 1 8 3 1 0 4 0 6 4
2021/2022122 1 0 0 0 1 1 1 2 20 9 27 60
2022/2023272 25 18 9 19 24 18 4 28 34 53 24 16
2023/2024263 24 32 28 15 20 13 3 56 0 10 40 22
2024/2025317 64 58 16 14 26 139 0 0 0 0 0 0
Totale 1.095