IRIS
MARTUCCIELLO, GIUSEPPE
 Distribuzione geografica
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Continente #
EU - Europa 19.526
Totale 19.526
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Nazione #
IT - Italia 19.526
Totale 19.526
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Città #
Genova 15.211
Rapallo 2.455
Genoa 1.751
Bordighera 62
Vado Ligure 47
Totale 19.526
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Nome #
L'esofagite distruttiva da caustici:trattamento chirurgico mediante esofago-colon-plastica sec.Waterston-Soave 286
Displasia neuronale intestinale e pseudo-malattia di Hirschsprung. 220
Neural crest neuroblasts can colonise aganglionic and ganglionic gut in vivo. 144
Histochemical study of Dom mouse: A model for Waardenburg-Hirschsprung's phenotype. 141
Abnormalities in "low" anorectal malformations (ARMs) and functional results resecting the distal 3 cm. 137
Preliminary report on the International Conference for the Development of Standards for the Treatment of Anorectal Malformations. 133
Gastrointestinal phenotype of ATR-X syndrome. 130
Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstruction. 129
HOX11L1: a promoter study to evaluate possible expression defects in intestinal motility disorders 126
Anorectal malformations associated with enteric dysganglionosis in Danforth's short tail (Sd) mice 123
Results of a mechanical Duhamel pull-through for the treatment of Hirschsprung's disease and intestinal neuronal dysplasia 120
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. 120
Update on basic research on Hirschsprung's disease. 120
Common PHOX2B poly-alanine contractions impair RET gene transcription, predisposing to Hirschsprung disease 120
Ret protein in the human fetal rectum. 119
A new rapid acetylcholinesterase histochemical method for the intraoperative diagnosis of Hirschsprung's disease and intestinal neuronal dysplasia 118
Mouse-isolated plexus differentiates neural crest precursors into enteric neuroblasts 117
Endocavitary electrocardiography during central vein catheter positioning in a newborn with persistent left superior vena cava. 117
[Computed tomography vs. magnetic resonance in the diagnosis of anorectal anomalies]. 115
A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10. 115
Diagnostic Criteria of Pediatric Intestinal Myopathies 115
10.5.9 Disganglionosi Intestinali Trattato di clinica e terapia V edizione 113
Hirschsprung's disease, one of the most difficult diagnoses in pediatric surgery: a review of the problems from clinical practice to the bench. 112
[Molecular biology, basic research and diagnosis of Hirschsprung's disease]. 112
Successful treatment of Neuroblastoma in an adolescent with intra-arterial embolization before surgery 112
Adrenal masses in children: the role of minimally invasive surgery. 110
Intestinal microvillous atrophy and transient neuronal dysplasia 109
Deleted and normal chromosome 10 homologs from a patient with Hirschsprung disease isolated in two cell hybrids through enrichment by immunomagnetic selection. 109
Rectal suction biopsy in the diagnosis of intestinal dysganglionoses: 5-year experience with Solo-RBT in 389 patients. 109
Associated anomalies in intestinal neuronal dysplasia 108
Perioperative management of hypertensive neuroblastoma: A study from the Italian Group of Pediatric Surgical Oncologists (GICOP) 107
Complete penoscrotal transposition. 106
GDNF deficit in Hirschsprung's disease. 105
CT of anorectal malformation--a postoperative evaluation. 104
HLXB9 homeobox gene and caudal regression syndrome. 103
La displasia neuronale intestinale tipo B migrant: una nuova entità clinica 102
Sacral development in anorectal malformations and in normal population 102
Anorectal malformations associated with sacral hypodevelopment: a spectrum of anomalies controlled by the same gene? 101
Molecular genetics of Hirschsprung disease. 101
Hirschsprung's disease: alpha-naphthylesterase activity in the enzyme-histochemical evaluation of the extent of the aganglionic segment during surgery 100
Autosomal recessive microcephaly with early onset seizures and spasticity. 100
Total colonic aganglionosis associated with an interstitial deletion of the long arm of chromosome 10. 99
Rectal suction biopsy in the workup of childhood chronic constipation: indications and diagnostic value. 99
Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation 98
Heterogeneity and low detection rate of RET mutations in Hirschsprung disease 98
Hirschsprung's Disease and Related neuromuscular Disorders of the Intestine 98
Video-Assisted Needle Core Biopsy in Children Affected by Neuroblastoma: A Novel Combined Technique 98
Association of multiple endocrine neoplasia type 2 and Hirschsprung disease. 97
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles 96
Use of staplers in congenital lobar emphysema. 96
Frequency of RET mutations in long- and short-segment Hirschsprung disease. 96
Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: report of a case with thumb hypoplasia. 95
Currarino syndrome: Proposal of a diagnostic and therapeutic protocol 92
Soave's extramucosal endorectal pull-through procedure. 92
Connective tissue in gut development: a key player in motility and in intestinal desmosis 92
Feasibility of perineal sagittal approaches in patients without anorectal malformations. 91
Laparoscopy in Diagnosis of Intestinal Motility Disorders 91
Genetics of anorectal malformations. 91
Histologic study of peritoneal adhesions in children and in a rat model 89
Hirschsprung's disease: alpha-naphthylesterase activity in the enzyme-histochemical evaluation of the extent of the aganglionic segment during surgery. 89
Complete Posterior Sagittal Anorectal Mobilization (PSAM): A new surgical approach for pediatric pelvic-perineal tumor resections 89
Neuronal intestinal dysplasia: clinical experience in Italian patients. 88
Perineal sagittal approach in patients without anorectal malformations 88
New concepts in preoperative imaging of anorectal malformation. New concepts in imaging of ARM. 88
Basic research on intestinal dysganglionosis 87
Hirschsprung disease: do risk factors of poor surgical outcome exist? 87
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease. 85
Histopathology of Chronic Constipation 85
Intraabdominal calcifications in the newborn: an unusual case with anorectal malformation and other anomalies. 85
[Blocked transcolostomy colonography in the identification of anorectal malformations]. 84
Long-gap oesophageal atresia: a combined endoscopic and radiologic evaluation. 82
Constipation and chronic intestinal pseudoobstruction as a clinical expression of intestinal neuronal dysplasia (IND)] 82
[Computed tomography and anorectal malformations. Their preoperative evaluation]. 81
Hirschsprung's disease: 13 Years' experience in 112 patients from a single institution 81
Abnormalities in low Anorectal Malformations (ARMs) and Functional Results Resecting the Distal Three Centimetres 80
Primary anastomosis in esophageal atresia type I without a gap 80
Preoperative enzymo-histochemical diagnosis of dysganglionoses associated with anorectal malformations (ARM) with recto-vestibular and recto-perineal fistula 80
Anorectal malformastions and hypothesis of mendelian inheritance 79
Myenteric Gangliositis in oesophageal achalasia of children 79
Exclusion of the Sonic Hedgeog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment 79
Single nucleotide polymorphic alleles in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's disease 78
Ingested magnets. 78
[Anesthesiologic approach in surgery of malformations in infants]. 77
A stray bullet in the brain. 77
One gene: different disorders: the concept of phenotype diversity due to allelic series. 77
Chicken Ovoalbumin Upstream Promoter Transcription Factor II in Mammalian Foetal Lung 76
[An association between anorectal malformations and Down's syndrome]. 76
Mapping and identification of a candidate gene for Hirschsprung disease:a review 75
A new enzymo-histochemical diagnosis kit for Hirschsprung disease. 75
HLXB9 and sacral agenesis and the Currarino syndrome 75
Update on molecular genetic research on Hirschsprung's disease 74
Total colonic aganglionosis associated with an interstitial deletion of the long arm of chromosome 10. Molecular characterization of the region and family studies 74
Immunohistochemical localization of RET protein in Hirschsprung's disease. 73
Diagnosi e trattamento chirurgico dell'aganglia totale del colon all'Istituto G.Gaslini 73
Condition for SSCP analysis, common polymorphisms and mutations of the RET protooncogene in Hirschsprung patients. 73
Total colonic aganglionosis. 73
Solo-RBT: a new instrument for rectal suction biopsies in the diagnosis of Hirschsprung's disease 73
Involvement of the HLXB9 homeobox gene in Currarino syndrome 73
Origin of PSAM procedure in surgical oncology 72
HLXB9, sacral agenesis and the Currarino syndrome. 71
Totale 9.949
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Categoria #
all - tutte 51.432
article - articoli 28.858
book - libri 193
conference - conferenze 18.020
curatela - curatele 0
other - altro 0
patent - brevetti 465
selected - selezionate 0
volume - volumi 3.896
Totale 102.864
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20205.846 0 86 299 224 503 398 1.306 255 413 1.264 689 409
2020/20211.065 51 77 57 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
2024/202566 55 11 0 0 0 0 0 0 0 0 0 0
Totale 19.644