IRIS
MARTUCCIELLO, GIUSEPPE
 Distribuzione geografica
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Continente #
EU - Europa 25.108
SA - Sud America 39
AS - Asia 36
AF - Africa 4
NA - Nord America 1
Totale 25.188
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Nazione #
IT - Italia 25.107
BR - Brasile 31
VN - Vietnam 15
CN - Cina 12
AR - Argentina 3
SG - Singapore 3
CL - Cile 2
ID - Indonesia 2
PY - Paraguay 2
ZA - Sudafrica 2
BD - Bangladesh 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CO - Colombia 1
HN - Honduras 1
IN - India 1
MA - Marocco 1
RU - Federazione Russa 1
TN - Tunisia 1
Totale 25.188
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Città #
Genova 15.211
Genoa 5.886
Rapallo 2.455
Vado Ligure 1.490
Bordighera 62
Ho Chi Minh City 5
Hanoi 4
Beijing 3
Singapore 3
Bari 2
Lấp Vò 2
Ninh Bình 2
Paulista 2
Rio de Janeiro 2
Santiago 2
São José do Rio Preto 2
São Paulo 2
Alta Floresta 1
Asunción 1
Bandar Seri Begawan 1
Barranquilla 1
Beberibe 1
Bragança Paulista 1
Buriticupu 1
Campo Grande 1
Cape Town 1
Caraguatatuba 1
Catanduva 1
Curitiba 1
Esteio 1
Ferryville 1
Fes 1
Guarujá 1
Guarulhos 1
Igaci 1
Jacobina 1
Joinville 1
Kazan' 1
Lomas de Zamora 1
Malang 1
Malhador 1
Manama 1
Mangaluru 1
Montalvânia 1
Neuquén 1
Nova Iguaçu 1
Pedra Azul 1
Pelotas 1
Piúma 1
Quilmes 1
Quixadá 1
Redenção 1
Saldanha 1
San Lorenzo 1
Sorocaba 1
Thái Bình 1
Totale 25.174
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Nome #
L'esofagite distruttiva da caustici:trattamento chirurgico mediante esofago-colon-plastica sec.Waterston-Soave 334
Displasia neuronale intestinale e pseudo-malattia di Hirschsprung. 249
Histochemical study of Dom mouse: A model for Waardenburg-Hirschsprung's phenotype. 172
Neural crest neuroblasts can colonise aganglionic and ganglionic gut in vivo. 167
Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstruction. 167
Abnormalities in "low" anorectal malformations (ARMs) and functional results resecting the distal 3 cm. 161
Anorectal malformations associated with enteric dysganglionosis in Danforth's short tail (Sd) mice 153
10.5.9 Disganglionosi Intestinali Trattato di clinica e terapia V edizione 153
Preliminary report on the International Conference for the Development of Standards for the Treatment of Anorectal Malformations. 152
Common PHOX2B poly-alanine contractions impair RET gene transcription, predisposing to Hirschsprung disease 152
Gastrointestinal phenotype of ATR-X syndrome. 151
HOX11L1: a promoter study to evaluate possible expression defects in intestinal motility disorders 149
Successful treatment of Neuroblastoma in an adolescent with intra-arterial embolization before surgery 148
A new rapid acetylcholinesterase histochemical method for the intraoperative diagnosis of Hirschsprung's disease and intestinal neuronal dysplasia 146
Diagnostic Criteria of Pediatric Intestinal Myopathies 146
[Computed tomography vs. magnetic resonance in the diagnosis of anorectal anomalies]. 144
Controversies concerning diagnostic guidelines for anomalies of the enteric nervous system: a report from the fourth International Symposium on Hirschsprung's disease and related neurocristopathies. 140
A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10. 139
Video-Assisted Needle Core Biopsy in Children Affected by Neuroblastoma: A Novel Combined Technique 139
Perioperative management of hypertensive neuroblastoma: A study from the Italian Group of Pediatric Surgical Oncologists (GICOP) 139
Update on basic research on Hirschsprung's disease. 138
Associated anomalies in intestinal neuronal dysplasia 136
Results of a mechanical Duhamel pull-through for the treatment of Hirschsprung's disease and intestinal neuronal dysplasia 136
Ret protein in the human fetal rectum. 134
[Molecular biology, basic research and diagnosis of Hirschsprung's disease]. 134
Mouse-isolated plexus differentiates neural crest precursors into enteric neuroblasts 133
Endocavitary electrocardiography during central vein catheter positioning in a newborn with persistent left superior vena cava. 131
Rectal suction biopsy in the workup of childhood chronic constipation: indications and diagnostic value. 130
Deleted and normal chromosome 10 homologs from a patient with Hirschsprung disease isolated in two cell hybrids through enrichment by immunomagnetic selection. 129
Rectal suction biopsy in the diagnosis of intestinal dysganglionoses: 5-year experience with Solo-RBT in 389 patients. 129
Neuronal intestinal dysplasia: clinical experience in Italian patients. 128
Hirschsprung's disease, one of the most difficult diagnoses in pediatric surgery: a review of the problems from clinical practice to the bench. 126
Adrenal masses in children: the role of minimally invasive surgery. 126
La displasia neuronale intestinale tipo B migrant: una nuova entità clinica 126
GDNF deficit in Hirschsprung's disease. 125
Histologic study of peritoneal adhesions in children and in a rat model 125
HLXB9 homeobox gene and caudal regression syndrome. 124
Intestinal microvillous atrophy and transient neuronal dysplasia 123
Complete penoscrotal transposition. 123
Molecular genetics of Hirschsprung disease. 123
Hirschsprung's Disease and Related neuromuscular Disorders of the Intestine 123
Total colonic aganglionosis associated with an interstitial deletion of the long arm of chromosome 10. 121
Hirschsprung's disease: alpha-naphthylesterase activity in the enzyme-histochemical evaluation of the extent of the aganglionic segment during surgery 121
Frequency of RET mutations in long- and short-segment Hirschsprung disease. 121
Soave's extramucosal endorectal pull-through procedure. 121
CT of anorectal malformation--a postoperative evaluation. 120
Currarino syndrome: Proposal of a diagnostic and therapeutic protocol 120
Sacral development in anorectal malformations and in normal population 120
Autosomal recessive microcephaly with early onset seizures and spasticity. 120
Complete Posterior Sagittal Anorectal Mobilization (PSAM): A new surgical approach for pediatric pelvic-perineal tumor resections 120
Anorectal malformations associated with sacral hypodevelopment: a spectrum of anomalies controlled by the same gene? 119
Preoperative enzymo-histochemical diagnosis of dysganglionoses associated with anorectal malformations (ARM) with recto-vestibular and recto-perineal fistula 119
Association of multiple endocrine neoplasia type 2 and Hirschsprung disease. 117
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles 115
Use of staplers in congenital lobar emphysema. 115
Hirschsprung's disease: alpha-naphthylesterase activity in the enzyme-histochemical evaluation of the extent of the aganglionic segment during surgery. 115
Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation 114
Perineal sagittal approach in patients without anorectal malformations 113
Connective tissue in gut development: a key player in motility and in intestinal desmosis 113
Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: report of a case with thumb hypoplasia. 112
Heterogeneity and low detection rate of RET mutations in Hirschsprung disease 112
Primary anastomosis in esophageal atresia type I without a gap 112
Constipation and chronic intestinal pseudoobstruction as a clinical expression of intestinal neuronal dysplasia (IND)] 111
Feasibility of perineal sagittal approaches in patients without anorectal malformations. 110
[An association between anorectal malformations and Down's syndrome]. 110
[Computed tomography and anorectal malformations. Their preoperative evaluation]. 108
Genetics of anorectal malformations. 108
Image-defined risk factors in unresectable neuroblastoma: SIOPEN study on incidence, chemotherapy-induced variation, and impact on surgical outcomes 108
Laparoscopy in Diagnosis of Intestinal Motility Disorders 107
20.18 Poliposi Familiare del Colon 107
Histopathology of Chronic Constipation 107
[Blocked transcolostomy colonography in the identification of anorectal malformations]. 106
Basic research on intestinal dysganglionosis 106
Hirschsprung's disease: 13 Years' experience in 112 patients from a single institution 106
Hirschsprung disease: do risk factors of poor surgical outcome exist? 105
CONSERVATIVE MANAGEMENT OF CHYLOUS ASCITES AFTER ONCOLOGICAL SURGERY FOR PERIPHERAL NEUROBLASTIC TUMORS IN PEDIATRIC PATIENTS 105
New concepts in preoperative imaging of anorectal malformation. New concepts in imaging of ARM. 104
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease. 103
Exclusion of the Sonic Hedgeog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment 103
Phenotypic variability of Dom mouse animal model of Hirschsprung's disease. 102
ROLE OF SURGERY IN NEUROBLASTOMA 4S : A CRITICAL UPDATE 100
A gene for Hirshsprung disease maps to the proximal long arm of chromosome 10 100
Intraabdominal calcifications in the newborn: an unusual case with anorectal malformation and other anomalies. 99
Ingested magnets. 99
Anorectal malformastions and hypothesis of mendelian inheritance 98
20.5.2 Addome Acuto 98
Single nucleotide polymorphic alleles in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's disease 97
[Anesthesiologic approach in surgery of malformations in infants]. 97
Long-gap oesophageal atresia: a combined endoscopic and radiologic evaluation. 97
A stray bullet in the brain. 97
Internal anal spincter in anorectal malformations myth or reality 97
Myenteric Gangliositis in oesophageal achalasia of children 96
Abnormalities in low Anorectal Malformations (ARMs) and Functional Results Resecting the Distal Three Centimetres 96
Choroba Hirschsprunga: aktywnosc alfa-naftyloesterazy wocenie enzymatycznohistochemicznej wialkosci odcinka Bezzwojowego jelita Grubego podczaz zabiegn operacyjnego 95
Diagnosi e trattamento chirurgico dell'aganglia totale del colon all'Istituto G.Gaslini 94
Condition for SSCP analysis, common polymorphisms and mutations of the RET protooncogene in Hirschsprung patients. 94
One gene: different disorders: the concept of phenotype diversity due to allelic series. 94
A new enzymo-histochemical diagnosis kit for Hirschsprung disease. 94
Involvement of the HLXB9 homeobox gene in Currarino syndrome 93
Hirschsprung's disease as a neurochristopathy. 92
Totale 12.306
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Categoria #
all - tutte 80.223
article - articoli 43.420
book - libri 288
conference - conferenze 29.704
curatela - curatele 0
other - altro 0
patent - brevetti 731
selected - selezionate 0
volume - volumi 6.080
Totale 160.446
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021880 0 0 0 98 46 101 65 113 159 117 88 93
2021/20222.965 55 264 244 407 86 134 179 642 119 315 58 462
2022/20232.993 334 119 43 303 477 509 31 258 533 38 301 47
2023/20241.252 125 238 43 107 92 116 64 96 62 19 60 230
2024/20253.568 55 371 113 207 477 370 310 431 148 206 402 478
2025/20262.160 673 161 673 653 0 0 0 0 0 0 0 0
Totale 25.306