Published in Ultrasound Obstet Gynecol on October 01, 2001
Prevalence of gastroschisis at birth: retrospective study. BMJ (2002) 1.42
Downregulation of ROCK-I and ROCK-II gene expression in the cadmium-induced ventral body wall defect chick model. Pediatr Surg Int (2008) 0.91
Disruption of calreticulin-mediated cellular adhesion signaling in the cadmium-induced omphalocele in the chick model. Pediatr Surg Int (2010) 0.90
HoxB2, HoxB4 and Alx4 genes are downregulated in the cadmium-induced omphalocele in the chick model. Pediatr Surg Int (2010) 0.90
Spontaneous intraamniotic hemorrhage in the second trimester mimicking an abdominal wall defect. J Turk Ger Gynecol Assoc (2013) 0.84
Review of the evidence on the closure of abdominal wall defects. Pediatr Surg Int (2010) 0.83
Gastroschisis and exomphalos in Ireland 1998-2004. Does antenatal diagnosis impact on outcome? Pediatr Surg Int (2007) 0.82
Effect of time to surgical evaluation on the outcomes of infants with gastroschisis. J Pediatr Surg (2012) 0.81
Perinatal mortality in pregnancies with omphalocele: data from the Chinese national birth defects monitoring network, 1996-2006. BMC Pediatr (2014) 0.80
Evaluating the time trends in prevalence of exomphalos in 14 cities of Liaoning province, 2006 to 2015. Sci Rep (2016) 0.80
Pre-treatment with N-acetylcysteine upregulates superoxide dismutase 2 and catalase genes in cadmium-induced oxidative stress in the chick omphalocele model. Pediatr Surg Int (2011) 0.79
Altered PITX2 and LEF1 gene expression in the cadmium-induced omphalocele in the chick model. Pediatr Surg Int (2011) 0.78
Disruption of GLI3-ZIC3 interaction in the cadmium-induced omphalocele chick model. Pediatr Surg Int (2011) 0.78
Management of Gastroschisis in a Peripheral Hospital. Med J Armed Forces India (2011) 0.75
Fetal abdominal wall defects--easy to diagnose--and then what? Ultrasound Obstet Gynecol (2001) 0.75
Gastroschisis: epidemiology and mode of delivery, 2005-2013. Am J Obstet Gynecol (2016) 0.75
Presenilin genes are downregulated during somitogenesis in the cadmium-induced omphalocele chick model. Pediatr Surg Int (2012) 0.75
BMPR1A-mediated BMP1 signalling is disrupted in the cadmium-induced omphalocele in the chick model. Pediatr Surg Int (2011) 0.75
Disturbance of SHH signalling pathway during early embryogenesis in the cadmium-induced omphalocele chick model. Pediatr Surg Int (2013) 0.75
Crystal structure of photosystem II from Synechococcus elongatus at 3.8 A resolution. Nature (2001) 6.21
The varicella zoster virus vasculopathies: clinical, CSF, imaging, and virologic features. Neurology (2008) 4.78
A novel procedure for quantitative polymerase chain reaction by coamplification of competitive templates. Gene (1992) 3.48
Stress doses of hydrocortisone reverse hyperdynamic septic shock: a prospective, randomized, double-blind, single-center study. Crit Care Med (1999) 3.20
Health-related quality of life and posttraumatic stress disorder in survivors of the acute respiratory distress syndrome. Crit Care Med (1998) 2.85
Genetic control of the CD4/CD8 T-cell ratio in humans. Nat Med (1995) 2.75
Analysis of HIV-1 load in blood, semen and saliva: evidence for different viral compartments in a cross-sectional and longitudinal study. AIDS (1996) 2.41
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011. Ultrasound Obstet Gynecol (2012) 2.38
Prenatal diagnosis of severe structural congenital malformations in Europe. Ultrasound Obstet Gynecol (2005) 2.19
Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: report of three patients. Am J Med Genet (1997) 2.17
Pregnancy outcome following maternal exposure to statins: a multicentre prospective study. BJOG (2012) 2.14
High vitamin A intake in early pregnancy and major malformations: a multicenter prospective controlled study. Teratology (1999) 2.12
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide. J Med Genet (2003) 2.03
Sexual transmission of the hepatitis C virus and efficacy of prophylaxis with intramuscular immune serum globulin. A randomized controlled trial. Arch Intern Med (1997) 1.92
The spectrum of congenital anomalies of the VATER association: an international study. Am J Med Genet (1997) 1.91
PCR based identification and discrimination of agents of mucormycosis and aspergillosis in paraffin wax embedded tissue. J Clin Pathol (2005) 1.89
Absolute quantitation of viremia in human immunodeficiency virus infection by competitive reverse transcription and polymerase chain reaction. J Clin Microbiol (1992) 1.85
Genome-wide scan for adult onset primary open angle glaucoma. Hum Mol Genet (2000) 1.82
Molecular profile of human immunodeficiency virus type 1 infection in symptomless patients and in patients with AIDS. J Virol (1992) 1.80
Molecular characterization of folate receptor 1 mutations delineates cerebral folate transport deficiency. Brain (2012) 1.77
Isolation of Mycoplasma arginini from commercial bovine sera and its implication in contaminated cell cultures. Proc Soc Exp Biol Med (1971) 1.75
B-cells are required for the initiation of insulitis and sialitis in nonobese diabetic mice. Diabetes (1997) 1.75
[German S3-guideline "Diagnosis and treatment of esophagogastric cancer"]. Z Gastroenterol (2011) 1.74
Quantitative fluorescence polymerase chain reaction for the rapid prenatal detection of common aneuploidies and fetal sex. Am J Obstet Gynecol (1997) 1.69
Effects of noninvasive positive pressure ventilatory support in non-COPD patients with acute respiratory insufficiency after early extubation. Intensive Care Med (1999) 1.62
Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease. Neurology (2007) 1.61
Recombination hotspot in NF1 microdeletion patients. Hum Mol Genet (2001) 1.61
The relationship between cognitive performance and employment and health status in long-term survivors of the acute respiratory distress syndrome: results of an exploratory study. Gen Hosp Psychiatry (2001) 1.54
The effect of stress doses of hydrocortisone during septic shock on posttraumatic stress disorder in survivors. Biol Psychiatry (2001) 1.52
Searching for psoriasis susceptibility genes in Italy: genome scan and evidence for a new locus on chromosome 1. J Invest Dermatol (1999) 1.50
Long-term outcome of children with acute cerebellitis. Neuropediatrics (2012) 1.50
Identification of a SUFU germline mutation in a family with Gorlin syndrome. Am J Med Genet A (2009) 1.49
CPPD crystal deposition disease in patients with rheumatoid arthritis. Clin Rheumatol (2005) 1.48
Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries. Eur J Med Genet (2005) 1.45
How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case. J Med Genet (1990) 1.44
Prevalence of mutations in TIGR/Myocilin in patients with adult and juvenile primary open-angle glaucoma. Am J Hum Genet (1998) 1.44
Respiratory findings in livestock farmworkers. J Occup Environ Med (2001) 1.43
Hemophilia and nonprogressing human immunodeficiency virus type 1 infection. Blood (1997) 1.41
Increased carbohydrate-deficient transferrin during pregnancy: relation to sex hormones. Alcohol Alcohol (1996) 1.40
Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1. Hum Mol Genet (2000) 1.38
Segregation of a 22 ring chromosome in three generations. Hum Genet (1983) 1.36
Diagnosis of invasive aspergillosis and mucormycosis in immunocompromised patients by seminested PCR assay of tissue samples. Eur J Clin Microbiol Infect Dis (2006) 1.35
The effect of stress doses of hydrocortisone during septic shock on posttraumatic stress disorder and health-related quality of life in survivors. Crit Care Med (1999) 1.35
A gene for achondroplasia-hypochondroplasia maps to chromosome 4p. Nat Genet (1994) 1.34
Analysis of ventricular shape by echocardiography in normal fetuses, newborns, and infants. Circulation (1983) 1.32
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC study. Eur J Hum Genet (1999) 1.32
Homozygous delta 32 deletion of the CCR-5 chemokine receptor gene in an HIV-1-infected patient. AIDS (1997) 1.32
Cerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome: a new phenotype. Neurology (2003) 1.27
Dynamics and modulation of human immunodeficiency virus type 1 transcripts in vitro and in vivo. J Virol (1996) 1.27
Detection of human immunodeficiency virus type 1 genomic RNA in plasma samples by reverse-transcription polymerase chain reaction. J Med Virol (1991) 1.26
Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15). J Med Genet (1980) 1.26
Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2. J Med Genet (2004) 1.25
Evaluation of prenatal diagnosis of congenital heart diseases by ultrasound: experience from 20 European registries. Ultrasound Obstet Gynecol (2001) 1.25
Dissection of human humoral immune response against hepatitis C virus E2 glycoprotein by repertoire cloning and generation of recombinant Fab fragments. Hepatology (1998) 1.21
Mapping B-cell epitopes of hepatitis C virus E2 glycoprotein using human monoclonal antibodies from phage display libraries. J Virol (2001) 1.19
High titre T antigen with minimal amounts of structural antigen in adenovirus-infected cells treated with hydroxyurea. Nature (1968) 1.19
Evaluation of the prenatal diagnosis of limb reduction deficiencies. EUROSCAN Study Group. Prenat Diagn (2000) 1.17
[I Brazilian Guidelines for cardiovascular prevention]. Arq Bras Cardiol (2013) 1.17
Adverse effects of prenatal methimazole exposure. Teratology (2001) 1.17
Quantitative molecular monitoring of human immunodeficiency virus type 1 activity during therapy with specific antiretroviral compounds. J Clin Microbiol (1995) 1.16
Pulmonary function and health-related quality of life in a sample of long-term survivors of the acute respiratory distress syndrome. Intensive Care Med (2000) 1.16
Molecular characterization and dynamics of hepatitis C virus replication in human fetal hepatocytes infected in vitro. Hepatology (1997) 1.15
Evolution of hypervariable region 1 of hepatitis C virus in primary infection. J Virol (1998) 1.13
Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletions. Hum Mutat (1999) 1.13
Gln368STOP myocilin mutation in families with late-onset primary open-angle glaucoma. Invest Ophthalmol Vis Sci (1998) 1.12
Quantitation of hepatitis C virus genome molecules in plasma samples. J Clin Microbiol (1994) 1.12
Ring chromosome 15:r(15). Identification by R banding. Humangenetik (1975) 1.11
Omphalocele and gastroschisis: a collaborative study of five Italian congenital malformation registries. Teratology (1993) 1.11
Genetic variation in transforming growth factor alpha: possible association of BamHI polymorphism with bilateral sporadic cleft lip and palate. Am J Hum Genet (1992) 1.09
Age, increased ocular and blood pressures, and retinal and disc fluorescein angiogram. Arch Ophthalmol (1980) 1.09
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes. Am J Hum Genet (2000) 1.09
Can retinoic acid ameliorate the physiologic and morphologic effects of elastase instillation in the rat? Chest (2000) 1.08
Nonneutralizing human antibody fragments against hepatitis C virus E2 glycoprotein modulate neutralization of binding activity of human recombinant Fabs. Virology (2001) 1.08
Usefulness of chromosome catalog in delineating new syndromes. Birth Defects Orig Artic Ser (1976) 1.08
Investigations on the pharmacokinetics of alpha-lipoic acid in healthy volunteers. Int J Clin Pharmacol Ther (1998) 1.07
Oral iloprost treatment in patients with Raynaud's phenomenon secondary to systemic sclerosis: a multicenter, placebo-controlled, double-blind study. Arthritis Rheum (1998) 1.05
Trans-activation of epidermal growth factor receptor gene by the hepatitis B virus X-gene product. Virology (1993) 1.04
Dynamics of molecular parameters of human immunodeficiency virus type 1 activity in vivo. J Virol (1994) 1.04
Time trends in neural tube defects prevalence in relation to preventive strategies: an international study. J Epidemiol Community Health (1999) 1.04
Host-specific modulation of the selective constraints driving human immunodeficiency virus type 1 env gene evolution. J Virol (1999) 1.04
Evaluation of the prenatal diagnosis of neural tube defects by fetal ultrasonographic examination in different centres across Europe. J Med Screen (2000) 1.03
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America. Hum Genet (2001) 1.03
Defective nef alleles in a cohort of hemophiliacs with progressing and nonprogressing HIV-1 infection. Virology (1999) 1.03
A randomized, controlled trial of a 24-month course of interferon alfa 2b in patients with chronic hepatitis B who had hepatitis B virus DNA without hepatitis B e antigen in serum. Hepatology (1997) 1.02
Active hepatitis C virus infection in bone marrow and peripheral blood mononuclear cells from patients with mixed cryoglobulinaemia. Clin Exp Immunol (1994) 1.02
Congenital diaphragmatic hernia: evaluation of prenatal diagnosis in 20 European regions. Ultrasound Obstet Gynecol (2002) 1.02
The safety of proton pump inhibitors in pregnancy: a multicentre prospective controlled study. Aliment Pharmacol Ther (2005) 1.02
Ionizing radiations in pregnancy and teratogenesis: a review of literature. Reprod Toxicol (2005) 1.02
Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype. Neuromuscul Disord (2008) 1.02
Spontaneous partial regression of low-grade glioma in children with neurofibromatosis-1: a real possibility. J Child Neurol (1999) 1.01
Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: a novel neurometabolic condition responding to folinic acid substitution. Neuropediatrics (2002) 1.01
Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: a case for "lumping". Am J Med Genet (1998) 1.01
Reduced folate transport to the CNS in female Rett patients. Neurology (2003) 1.00