779 results on '"Perrotta, S"'
Search Results
202. High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis
203. Frequent de novomutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio
204. αI/65 Hereditary elliptocytosis in Southern Italy: Evidence for an African origin
205. Early rectal cancer: Local excision by Trans-anal Endoscopic Microsurgery (T.E.M.)
206. Rotture Traumatiche della milza e lesioni associate
207. Occlusione intestinale da carcinoma del grosso intestino
208. Management of the risk for severe infections in children with asplenia: Recommendations from the Italian Network of Asplenia,La gestione del rischio infettivo nei bambini asplenici: Raccomandazioni dal network italiano asplenia
209. Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potential
210. Geographic distribution of CDA-II: Did an founder effect operate in Southern Italy?
211. Sickle cell disease at the emergency unit,La malattia drepanocitica in pronto soccorso: Algoritmo interattivo diagnostico-Terapeutico per la gestione degli eventi acuti
212. Is 1 mm thickness sec. Breslow the correct cut-off for sentinel node biopsy in melanoma? Report of six cases of metastasis by thin melanoma
213. P134: THE AREAL PROJECT: A VIRTUAL REALITY APPLICATION TO SUPPORT THE THERAPEUTIC EXPERIENCE AND THERAPY EDUCATION OF ADULT PATIENTS WITH THALASSEMIA AND SICKLE CELL DISEASE
214. Genetic heterogeneity of congenital dyserythropoietic anemia type II [3]
215. Cardiac transplant vasculopathy treated by percutaneous coronary intervention
216. Myocardial iron is strongly associated with reproductive function in beta-thalassemic women under chelation therapy
217. Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: Band 3 vesuvio [3]
218. Increased membrane protein phosphorylation and anion transport activity in chorea-acanthocytosis
219. Comparison of LIC obtained from biopsy, BLS and R(2)-MRI in iron overloaded patients with beta-thalassemia, treated with deferasirox (Exjade (R), ICL670)
220. Inherited disorders of bilirubin metabolism,Disordini ereditari del metabolismo della bilirubina
221. Deferasirox: The optimal chelation in transfusion-dependent anemias,Deferasirox: La chelazione ottimale nelle anemie trasfusione-dipendenti
222. Surgical treatment of pericardial cyst through median sternotomy
223. Hereditary spherocytosis (HS) due to loss of anion exchange transporter
224. Le anemie diseritropoietiche
225. Molecular basis of inherited bilirubin disorders in pediatrics
226. The Italian SurveY on carDiac rEhabilitation 2008 (ISYDE 2008): Study presentation,Il progetto ISYDE 2008 (Italian SurveY on carDiac rEhabilitation): Strutture, rete, organizzazione e programmi di cardiologia riabilitativa in Italia
227. P16~I~N~K~4 gene deletions in childhood acute lymphoblastic leukemias
228. Isolated Kommerells aneurysm in Turners syndrome
229. A Rapid Method for the Detection of AlphaI'65 Hereditary Elliptocytosis.
230. WHEN TO ADDRESS MOLECULAR STUDIES IN RED CELL MEMBRANE DEFECTS
231. Oral clinical manifestations of neurofibromatosis type 1 in children and adolescents
232. THE PROBLEM OF RECESSIVE HEREDITARY SPHEROCYTOSIS (HS)
233. 60 EVALUATION OF ANKYRIN CONTENT IN HEREDITARY SPHEROCYTOSIS
234. Functional outcome after laparoscopic posterior rectopexy for rectal prolapse
235. 103 CLINICAL AND GENETIC HETEROGENEITY OF RECESSIVE FORM OF HEREDITARY SPHEROCYTOSIS
236. A TRUNCATED ß-SPECTRIN (202 kD) ASSOCIATED WITH HS AND ISOLATED SPECTRIN DEFICIENCY 122
237. Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene
238. The 3He+5He→α+α reaction below the Coulomb barrier via the Trojan Horse Method.
239. Study of the quasi-free 3He+9Be→3α reaction for the Trojan Horse Method.
240. The 10B(n,α)7Li cross sections at ultra-low energy through the Trojan Horse Method applied to the 2H(10B,α7Li)1H.
241. Nuclear AstroPhysics Experiments with Trojan Horse Method.
242. Clinical outcome of transfusions with extended red blood cell matching in β-thalassemia patients: A single-center experience.
243. Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-thalassemia
244. Multiple spinal nerve enlargement and SOS1 mutation: Further evidence of overlap between neurofibromatosis type 1 and Noonan phenotype.
245. The interactome of the N-terminus of band 3 regulates red blood cell metabolism and storage quality
246. Phase 2 study for nonmetastatic extremity high-grade osteosarcoma in pediatric and adolescent and young adult patients with a risk-adapted strategy based on ABCB1/P-glycoprotein expression: An Italian Sarcoma Group trial (ISG/OS-2)
247. Non-transfusion-dependent thalassemia in Italy: less blues, no role of reds
248. Pseudo Hemifacial Microsomia With Condylar-Coronoid Collapse: New Therapeutic Approach in Growing Patients
249. Effects of Germline VHL Deficiency on Growth, Metabolism, and Mitochondria
250. Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric Study
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