Published in Pathologica on September 30, 1993
Progressive pseudorheumatoid dysplasia: report of a family and review. J Med Genet (1997) 1.20
Dominantly inherited progressive pseudorheumatoid dysplasia with hypoplastic toes. Skeletal Radiol (2004) 0.95
Endoscopic management of foreign bodies in the upper gastrointestinal tract: report on a series of 414 adult patients. Endoscopy (2001) 1.73
Miniaturized flow cytometry-based BCR-ABL immunoassay in detecting leptomeningeal disease. Leuk Res (2011) 1.40
Acute megakaryoblastic leukemia: experience of GIMEMA trials. Leukemia (2002) 1.22
Vertebral and costal osteochondromas causing spinal cord compression. Am J Roentgenol Radium Ther Nucl Med (1975) 1.20
Prevalence of thyroid disorders in untreated adult celiac disease patients and effect of gluten withdrawal: an Italian multicenter study. Am J Gastroenterol (2001) 1.12
Acute lymphoblastic leukaemia occurring as second malignancy: report of the GIMEMA archive of adult acute leukaemia. Gruppo Italiano Malattie Ematologiche Maligne dell'Adulto. Br J Haematol (1999) 1.07
[Use of 5-butyl-1-cyclohexyl-2,4,6,-trioxoperidropyrimidine (BCP) in the prevention and therapy of neonatal hyperbilirubinemia. Comparative study with phenobarbital]. Minerva Pediatr (1976) 1.07
Hand images: normal and abnormal. J Nucl Med (1977) 0.95
Clinical and biological features of acute myeloid leukaemia occurring as second malignancy: GIMEMA archive of adult acute leukaemia. Br J Haematol (2001) 0.94
Birth prevalence of skeletal dysplasias in the Italian Multicentric Monitoring System for Birth Defects. Prog Clin Biol Res (1982) 0.93
Treatment of adults with acute lymphoblastic leukaemia in first bone marrow relapse: results of the ALL R-87 protocol. Br J Haematol (1997) 0.92
Characterization of two novel cell lines, DERL-2 (CD56+/CD3+/Tcry5+) and DERL-7 (CD56+/CD3-/TCRgammadelta-), derived from a single patient with CD56+ non-Hodgkin's lymphoma. Leukemia (2001) 0.91
Sponastrime dysplasia: report on a male patient. Pediatr Radiol (1994) 0.91
Immunophenotype of acute lymphoblastic leukemia cells: the experience of the Italian Cooperative Group (Gimema). Leuk Lymphoma (1993) 0.90
Holt Oram syndrome associated with carcinoma. Clin Radiol (1971) 0.89
Pitfalls of genetic counselling in brachydactyly type C. Am J Med Genet (1994) 0.86
F-syndrome (F-form of acro-pectoro-vertebral dysplasia): report on a second family. Am J Med Genet (1995) 0.86
Hereditary enlarged parietal foramina (foramina parietalia permagna). Prenatal diagnosis, evolution and family study. Pathologica (1986) 0.86
Brachyphalangy, feet polydactyly, absent/hypoplastic tibiae: a further case and review of main diagnostic findings. Clin Dysmorphol (2001) 0.86
Sponastrime dysplasia: report on two siblings with metal retardation. Pediatr Radiol (1993) 0.85
Sertraline treatment for premature ejaculation. J Clin Psychopharmacol (1995) 0.84
Ear malformation in baby born to mother using tretinoin cream. Lancet (1992) 0.84
Acropectorovertebral dysgenesis (F syndrome) maps to chromosome 2q36. J Med Genet (2004) 0.84
New X linked spondyloepimetaphyseal dysplasia: report on eight affected males in the same family. J Med Genet (1994) 0.82
Hb-M "Hyde Park": a de novo mutation, identified by mass spectrometry and DNA analysis. Haematologica (1992) 0.82
Giant sigmoidal diverticulum: report of a case and review of the literature. Dis Colon Rectum (1978) 0.82
Partial deletions of long arm of chromosome 6: biologic and clinical implications in adult acute lymphoblastic leukemia. Leukemia (2002) 0.82
[Gorlin-Goltz syndrome with odontogenic keratosis. Report on a patient followed for 10 years]. Minerva Stomatol (1995) 0.82
Congenital hypertrichosis, cardiomegaly, and osteochondrodysplasia (Cantú syndrome): a new case with unusual radiological findings. Am J Med Genet (2000) 0.82
Synpolydactyly (type II syndactyly) with aplasia/hypoplasia of the middle phalanges of the toes: report on a family with eight affected members in four generations. Am J Med Genet (1995) 0.82
Bone scan in mastocytosis: case report. J Nucl Med (1976) 0.81
Oral-facial-digital syndrome: report on a transitional type between the Mohr and Váradi syndromes in a fetus. Am J Med Genet (1994) 0.81
Characteristics of secondary acute lymphoblastic leukemia with L3 morphology in adult patients. Leuk Lymphoma (2002) 0.80
Prevalence of valvular regurgitation in structurally normal hearts: a colour-Doppler study. Coron Artery Dis (1998) 0.80
A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis. Clin Genet (1997) 0.79
[Pseudoachondrodysplasia (pseudoachondroplastic spondyloepiphyseal dysplasia). Description of 2 non-familial cases]. Pathologica (1990) 0.79
[Oromandibular-limb hypogenesia spectrum: report of a case of lower ankylogloxia ++ associated with bilateral apodia]. Pathologica (1994) 0.79
Antenatal ultrasonographic diagnosis of a proximal femoral focal deficiency. J Clin Ultrasound (1993) 0.79
Phenotypic comparison of an osteogenesis imperfecta type IV proband with a de novo alpha2(I) Gly922 --> Ser substitution in type I collagen and an unrelated patient with an identical mutation. Biochem Mol Med (1997) 0.79
Evidence of a hypercoagulable state in patients with acute lymphoblastic leukemia treated with low dose of E. coli L-asparaginase: a GIMEMA study. Thromb Haemost (1993) 0.79
New multisystemic disorder involving heart valves, skin, bones, and joints in two brothers. Am J Med Genet (1993) 0.78
GIMEMA ALL 0288: a multicentric study on adult acute lymphoblastic leukemia. Preliminary results. Leukemia (1992) 0.78
Expression of GALT in two unrelated 9p- patients. Evidence for assignment of the GALT locus to the 9p21 band. Hum Genet (1981) 0.78
Prenatal diagnosis of thanatophoric dysplasia at 24 weeks. Am J Med Genet (1984) 0.78
Hemothorax: unusual complication of hereditary multiple exostosis. N Y State J Med (1981) 0.77
Early detection by ultrasound scan of severe post-chemotherapy gut complications in patients with acute leukemia. Haematologica (1999) 0.77
Kinetics of serum TK and LDH during therapy for AML. Haematologica (1990) 0.77
An unusual radiological finding in thanatophoric dysplasia type 1 with common mutation of the fibroblast growth factor receptor-3 (FGFR3) gene (Arg248Cys) Am J Med Genet (1997) 0.77
Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance. Clin Dysmorphol (1993) 0.76
[New case of thanatophoric dwarfism associated with cloverleaf skull]. Pathologica (1975) 0.76
In vivo measurement of human lens aging using the lens opacity meter. Ophthalmologica (1989) 0.76
[Polimorphonuclear leukocytes and diabetes mellitus]. Minerva Med (2008) 0.76
Serum thymidine kinase peaks early during AML induction therapy. Leukemia (1989) 0.75
[Association of a clover-leaf skull associated with thanaphoric nanism (1st case in Italian literature)]. Pathologica (1974) 0.75
[Methemoglobinemia in the newborn and nursing infant. Genetic and acquired forms. Personal case list]. Pathologica (1987) 0.75
CD10/common acute lymphoblastic leukemia-associated antigen and adhesion factor expression is predictive for lymphokine-activated killing sensitivity of adult B-lineage acute lymphoblastic leukemia. Year Immunol (1993) 0.75
Double-blind evaluation of the safety and hypnotic efficacy of lormetazepam in general practice. Clin Ther (1983) 0.75
[Further note on the xeroradiographic study of soft tissue tumors in childhood]. Radiol Med (1979) 0.75
Acute self-limited colitis complicating diagnostic colonoscopy. Am J Gastroenterol (2001) 0.75
[X-ray aspect of the lumbar spine in mongoloid newborn infants (proceedings)]. Radiol Med (1978) 0.75
[Gingival hypertrophy in I-cell disease (mucolipidosis II). A report of 2 nonfamilial cases. II]. Minerva Stomatol (1993) 0.75
[A case of Zellweger's cerebro-hepato-renal syndrome]. Minerva Pediatr (1977) 0.75
[Achondrogenesis and thanatophoric nanism. Clinical, radiological and genetic aspects]. Minerva Pediatr (1976) 0.75
[Histological and histochemical study of structural changes of the capillaries in the synovial membrane during aspecific phlogosis]. Chir Organi Mov (1966) 0.75
The Takagi Automatic Tangent Screen ATS-85 analyzer for the detection of glaucomatous patients. Ann Ophthalmol (1991) 0.75
[Determination of adenosine-deaminase activity in the blood in a group of infants with Salmonella typhimurium infection]. Pathologica (1974) 0.75
Spin polarized surface resonance bands in single layer Bi on Ge(1 1 1). J Phys Condens Matter (2016) 0.75
[Ventricular diastole in progressive systemic sclerosis]. Recenti Prog Med (1994) 0.75
[Aplasia cutis congenita and fetus papyraceus]. Minerva Pediatr (1982) 0.75
Porphyria cutanea tarda and hematological diseases. Am J Hematol (1988) 0.75
[Prenatal diagnosis of thanatophoric dysplasia at 21st week of pregnancy]. Pathologica (1993) 0.75
Type A2 brachydactily: report of a new family. Acta Genet Med Gemellol (Roma) (1977) 0.75
Daunomycin--preliminary results of the treatment of acute leukemias in adults. Oncology (1968) 0.75
[Camurati-Engelmann disease. Description of 2 related cases. Therapeutic approach with peridural anesthesia]. Pathologica (1987) 0.75
[Hepatic symmetry as radiological sign of asplenia, polysplenia and M-anisosplenia]. Minerva Pediatr (1976) 0.75
Previous occurrence of life-threatening abdominal infection is not a contraindication to bone marrow transplantation. Haematologica (1999) 0.75
Complete phenotypic and genotypic lineage switch in a Philadelphia chromosome-positive acute lymphoblastic leukemia. Leukemia (1996) 0.75
Severe pancytopenia and intrahepatic cholestasis in a patient with a history of Hodgkin's disease. Responsiveness to high-dose pulse steroid therapy and diagnosis of a late relapse. Eur J Intern Med (2001) 0.75
[Congenital defects caused by amniotic bands]. Pathologica (1985) 0.75
[Dental abnormalities in cleidocranial dysplasia. Presentation of 4 cases]. Pathologica (1993) 0.75
[Campomelic dwarfism. Re-examination of our study]. Minerva Pediatr (1976) 0.75
[Not Available]. Acta Haematol (1955) 0.75
[Prenatal results in genetic osteochondrodysplasia. Diagnostic protocol]. Pathologica (1987) 0.75
Ultrasound scan to detect acalculous cholecystopathy in immunocompromised hosts with unexplained fever. Haematologica (2000) 0.75
[Study of a case of histiocytosis X in an infant]. Pathologica (1974) 0.75
[Case of achondrogenesis (Parenti's disease). Possible relationship to tanaphoric nanism]. Pathologica (1974) 0.75
Central venous catheter insertion: a bedside procedure for haematological patients. Eur J Haematol (1996) 0.75
[Pharyngo-esophageal achalasia in the newborn infant]. Minerva Pediatr (1976) 0.75
[Xeroradiography in the study of tumors of the soft parts in childhood]. Radiol Med (1979) 0.75
[Prognostic factors ascertained and correlated in the study of adult lymphoblastic leukemia]. Haematologica (1989) 0.75
[Autosomal dominant chondrodysplasia punctata with laryngo-tracheal calcification. Presentation of 2 cases]. Pathologica (1987) 0.75
[Oculodentodigital dysplasia: report of 2 familial cases]. Pathologica (1994) 0.75
Familiar B-cell neoplasms and HLA antigens. Haematologica (1986) 0.75
[Fronto-nasal dysplasia. Personal case]. Pathologica (1974) 0.75
CD7(+) acute leukemia switching from a lymphoid to a myeloid phenotype. Haematologica (2001) 0.75
Serum pseudouridine in the diagnosis of acute leukaemias and as a novel prognostic indicator in acute lymphoblastic leukaemia. Clin Biochem (1993) 0.75
[The so-called "thanatophoric dwarfism". Personal contribution]. Minerva Pediatr (1969) 0.75
[Isolated macrodactyly or extremely circumscribed Proteus syndrome?]. Pathologica (1994) 0.75