Published in Berl Munch Tierarztl Wochenschr on September 01, 1997
Has the impact of heat waves on mortality changed in France since the European heat wave of summer 2003? A study of the 2006 heat wave. Int J Epidemiol (2008) 3.82
Current practice of temporary vena cava filter insertion: a multicenter registry. J Vasc Interv Radiol (2000) 2.00
Decline in semen concentration and morphology in a sample of 26,609 men close to general population between 1989 and 2005 in France. Hum Reprod (2012) 1.67
Clinical and economic impact of infusion reactions in patients with colorectal cancer treated with cetuximab. Ann Oncol (2010) 1.66
Prenatal diagnosis of alpha-1-antitrypsin deficiency using oligonucleotide probe analysis. Hum Genet (1988) 1.63
Efficacy of tetracaine-adrenaline-cocaine topical anesthetic without tetracaine for facial laceration repair in children. Pediatrics (1990) 1.63
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker. Genomics (1989) 1.59
Results on neutrinoless double-β decay of 76Ge from phase I of the GERDA experiment. Phys Rev Lett (2013) 1.54
The effect of oral midazolam on anxiety of preschool children during laceration repair. Ann Emerg Med (1990) 1.46
Haemophilia B: database of point mutations and short additions and deletions--third edition, 1992. Nucleic Acids Res (1992) 1.36
Short-term associations between fine and coarse particles and hospital admissions for cardiorespiratory diseases in six French cities. Occup Environ Med (2007) 1.31
Haemophilia B: database of point mutations and short additions and deletions--second edition. Nucleic Acids Res (1991) 1.29
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene. Nucleic Acids Res (1991) 1.26
Phenylketonuria: distribution of DNA diagnostic patterns in German families. Hum Genet (1988) 1.24
A somatic mosaic for haemophilia A detected at the DNA level. Mol Biol Med (1988) 1.21
Efficacy of silver-coated fabric to prevent bacterial colonization and subsequent device-based biofilm formation. J Biomed Mater Res (2000) 1.21
Entities and frequency of neonatal diabetes: data from the diabetes documentation and quality management system (DPV). Diabet Med (2010) 1.20
Characterization of mutations in the factor VIII gene by direct sequencing of amplified genomic DNA. Genomics (1990) 1.20
Haemophilia B: database of point mutations and short additions and deletions. Nucleic Acids Res (1990) 1.20
Dispersed rat parotid acinar cells. II. Characterization of adrenergic receptors. Am J Physiol (1975) 1.18
Forensic DNA-typing of dog hair: DNA-extraction and PCR amplification. Forensic Sci Int (2004) 1.16
A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease. Genomics (1993) 1.15
Recovery from hemophilia B Leyden: an androgen-responsive element in the factor IX promoter. Science (1992) 1.14
Quantitative trait loci mapping of functional traits in the German Holstein cattle population. J Dairy Sci (2003) 1.13
Elliptic flow of charged particles in Pb-Pb collisions at sqrt[S(NN)] = 2.76 TeV. Phys Rev Lett (2010) 1.12
The molecular basis of alpha 1-antichymotrypsin deficiency in a heterozygote with liver and lung disease. J Hepatol (1993) 1.12
Particle-yield modification in jetlike azimuthal dihadron correlations in Pb-Pb collisions at √s(NN)=2.76 TeV. Phys Rev Lett (2012) 1.11
Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies. Am J Hum Genet (1996) 1.10
A linkage map of the porcine genome from a large-scale White Duroc x Erhualian resource population and evaluation of factors affecting recombination rates. Anim Genet (2009) 1.10
Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis. Proc Natl Acad Sci U S A (1991) 1.08
Transverse momentum distribution and nuclear modification factor of charged particles in p+Pb collisions at sqrt[s(NN)] = 5.02 TeV. Phys Rev Lett (2013) 1.08
Haemophilia A: mutation type determines risk of inhibitor formation. Thromb Haemost (1995) 1.07
Higher harmonic anisotropic flow measurements of charged particles in Pb-Pb collisions at sqrt(s(NN)) = 2.76 TeV. Phys Rev Lett (2011) 1.05
Somatic mosaicism in hemophilia A: a fairly common event. Am J Hum Genet (2001) 1.03
Serum immunoglobulins and coproantibody formation in infants after artificial intestinal colonization with Escherichia coli 083 and oral lysozyme administration. Pediatr Res (1973) 1.03
Methylation levels at selected CpG sites in the factor VIII and FGFR3 genes, in mature female and male germ cells: implications for male-driven evolution. Am J Hum Genet (1998) 1.01
Parental origin of factor IX gene mutations, and their distribution in the gene. Am J Hum Genet (1992) 1.01
Isolation of fecal coliform bacteria from the diamondback terrapin (Malaclemys terrapin centrata). Appl Environ Microbiol (1999) 1.01
Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome 7. Am J Hum Genet (1987) 1.00
DNA polymorphisms of the alpha 1-antitrypsin gene region in patients with chronic obstructive pulmonary disease. Eur J Clin Invest (1990) 0.99
Allelic dimorphism in the human tissue-type plasminogen activator (TPA) gene as a result of an Alu insertion/deletion event. Hum Genet (1992) 0.99
Seattle YouthCare's prevention, intervention, and education program: a model of care for HIV-positive, homeless, and at-risk youth. J Adolesc Health (1998) 0.98
Production of muons from heavy flavor decays at forward rapidity in pp and Pb-Pb collisions at sqrt[s(NN)]=2.76 TeV. Phys Rev Lett (2012) 0.98
Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa. Genomics (1991) 0.98
A human single-copy DNA probe (DR 47) detects a Taq I RFLP on chromosome 9 (D9S5). Nucleic Acids Res (1987) 0.97
A genome-wide scan reveals candidate susceptibility loci for pig hernias in an intercross between White Duroc and Erhualian. J Anim Sci (2009) 0.96
Efficacy of TAC topical anesthetic for repair of pediatric lacerations. Am J Dis Child (1988) 0.96
Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B. Am J Hum Genet (1989) 0.95
Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung disease. Lancet (1992) 0.95
Hypophosphatemic rickets with hypercalciuria due to mutation in SLC34A3/NaPi-IIc can be masked by vitamin D deficiency and can be associated with renal calcifications. Exp Clin Endocrinol Diabetes (2008) 0.95
De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism. Blood (2000) 0.94
Mapping of QTL for Body Conformation and Behavior in Cattle. J Hered (2003) 0.93
Centrality dependence of the charged-particle multiplicity density at midrapidity in Pb-Pb collisions at sqrt[s(NN)] = 2.76 TeV. Phys Rev Lett (2011) 0.93
Regeneration-associated high level expression of apolipoprotein D mRNA in endoneurial fibroblasts of peripheral nerve. EMBO J (1990) 0.93
Transformation of lymphocytes in patients with certain bacterial infections. Med Microbiol Immunol (1975) 0.93
Molecular defects in hemophilia A: identification and characterization of mutations in the factor VIII gene and family analysis. Blood (1989) 0.92
Polymorphisms in MHC-DRA and -DRB alleles of water buffalo (Bubalus bubalis) reveal different features from cattle DR alleles. Anim Genet (2003) 0.92
Recurrent mutations in the factor IX gene: founder effect or repeat de novo events. Investigation of the German haemophilia B population and review of de novo mutations. Hum Genet (1993) 0.92
Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M allele. Am J Hum Genet (1994) 0.91
cDNA cloning and sequencing of the human ryanodine receptor type 3 (RYR3) reveals a novel alternative splice site in the RYR3 gene. FEBS Lett (1998) 0.90
Mobile diabetes education and care: intervention for children and young people with Type 1 diabetes in rural areas of northern Germany. Diabet Med (2006) 0.89
Cystic fibrosis: typing 48 German families with linked DNA probes. Hum Genet (1987) 0.89
Chromosomal anchoring of linkage groups and identification of wing size QTL using markers and FISH probes derived from microdissected chromosomes in Nasonia (Pteromalidae: Hymenoptera). Cytogenet Genome Res (2004) 0.88
Compound heterozygotes in hyperphenylalaninaemia. Hum Genet (1984) 0.88
Identification and characterization of novel peroxisome proliferator-activated receptor-gamma (PPAR-gamma) transcriptional variants in pig and human. J Anim Breed Genet (2005) 0.88
Construction and characterization of a porcine P1-derived artificial chromosome (PAC) library covering 3.2 genome equivalents and cytogenetical assignment of six type I and type II loci. Mamm Genome (1999) 0.88
Zinc finger proteins: watchdogs in muscle development. Mol Gen Genet (1999) 0.88
Low genetic variability and strong differentiation among isolated populations of the rare steppe grass Stipa capillata L. in Central Europe. Plant Biol (Stuttg) (2010) 0.88
Midrapidity antiproton-to-proton ratio in pp collisons at sqrt[s]=0.9 and 7 TeV measured by the ALICE experiment. Phys Rev Lett (2010) 0.87
Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia A. Am J Hum Genet (1993) 0.87
Implication of complex vertebral malformation and bovine leukocyte adhesion deficiency DNA-based testing on disease frequency in the Holstein population. J Dairy Sci (2008) 0.86
Characterization of mutations within the factor VIII gene of 73 unrelated mild and moderate haemophiliacs. Br J Haematol (1995) 0.86
Multiple consequences of human growth hormone expression in transgenic mice. Mol Biol Med (1989) 0.86
Restriction site mapping of adenovirus types 9 and 15 and genome types of intermediate adenovirus 15/H9. Intervirology (1989) 0.86
Detection of classical and atypical/Nor98 scrapie by the paraffin-embedded tissue blot method. Vet Rec (2009) 0.86
Diagnostic difficulties in glucokinase hyperinsulinism. Horm Metab Res (2008) 0.85
Genomic structure and nucleotide polymorphisms of the porcine agouti signalling protein gene (ASIP). Anim Genet (2000) 0.84
Haemophilia B+ with inhibitor. Thromb Haemost (1988) 0.84
Identification of a mutation in the ovine uroporphyrinogen decarboxylase (UROD) gene associated with a type of porphyria. Anim Genet (2005) 0.83
Mutations in severe hemophilia A: distribution within the factor VIII gene, origin and influence on inhibitor development. Beitr Infusionsther Transfusionsmed (1997) 0.83
Prenatal diagnosis of haemophilia B by the use of polymerase chain reaction and direct sequencing. Klin Wochenschr (1991) 0.83
Detection and characterisation of two missense mutations at a cleavage site in the factor VIII light chain. Thromb Res (1991) 0.83
Sequence-based typing reveals a novel DLA-88 allele, DLA-88*04501, in a beagle family. Tissue Antigens (2006) 0.83
Highly variable clinical course in severe alpha 1-antitrypsin deficiency--use of polymerase chain reaction for the detection of rare deficiency alleles. Klin Wochenschr (1990) 0.82
Development of faecal immunoglobulins and coproantibodies in infants after artificial oral colonization with E. coli 083. Experientia (1970) 0.82
DNA polymorphisms associated with a new alpha 1-antitrypsin PIQ0 variant (PIQ0riedenburg). Hum Genet (1991) 0.82
J/ψ elliptic flow in Pb-Pb collisions at √(s(NN))=2.76 TeV. Phys Rev Lett (2013) 0.82
Cystic fibrosis: typing 89 German families with linked DNA probes. Hum Genet (1988) 0.82
Isolation and characterization of microsatellite marker loci in the greylag goose (Anser anser). Mol Ecol Resour (2008) 0.82
Immunological profiles in workers occupationally exposed to inorganic mercury. J Hyg Epidemiol Microbiol Immunol (1990) 0.82
Transgenic pigs carrying cDNA copies encoding the murine Mx1 protein which confers resistance to influenza virus infection. Gene (1992) 0.81
Hemophilia B caused by five different nondeletion mutations in the protease domain of factor IX. Blood (1992) 0.81
Identical point mutations in the factor VIII gene that have different clinical manifestations of hemophilia A. Am J Hum Genet (1990) 0.81
Comparison between intratracheal and intravenous administration of liposome-DNA complexes for cystic fibrosis lung gene therapy. Gene Ther (1998) 0.81
The porcine skeletal muscle ryanodine receptor gene structure coding region 1 to 10614 harbouring 71 exons. Anim Genet (1996) 0.81
Molecular characterization and chromosomal assignment of the canine protein C gene. Mamm Genome (1999) 0.81
Pseudorapidity density of charged particles in p+Pb collisions at √(s(NN))=5.02 TeV. Phys Rev Lett (2013) 0.81
Evidence for human chorionic gonadotropin binding sites in some organs of the immature female rat--effect of non-labelled chorionic gonadotropin and follicle-stimulating hormone on the distribution of 125-I-labelled human chorionic gonadotropin. Folia Morphol (Praha) (1971) 0.81
Assignment of the phosphoglycerate kinase 1 (PGK1) gene to porcine chromosome Xq12-q13 by fluorescence in situ hybridization and hybrid panel analyses. Anim Genet (2004) 0.80
Cloning of the human alpha 2-macroglobulin gene and detection of mutations in two functional domains: the bait region and the thiolester site. Hum Genet (1992) 0.80