Published in Eur J Pediatr Surg on April 01, 2006
Transanal endorectal pull-through for Hirschsprung's disease using long cuff dissection and short V-shaped partially resected cuff anastomosis: early and late outcomes. Pediatr Surg Int (2012) 0.83
Transanal one-stage endorectal pull-through for Hirschsprung disease: experiences with 51 newborn patients. Pediatr Surg Int (2010) 0.75
Primary transanal Swenson pull-through operation for Hirschsprung's disease. Pediatr Surg Int (2009) 0.75
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. Hum Mol Genet (1997) 3.26
The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules. J Cell Sci (2005) 2.86
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family. Nat Genet (1997) 2.68
Tuberculosis treatment programmes in low-income countries. Lancet (1994) 2.31
Regulation of pim and myb mRNA accumulation by interleukin 2 and interleukin 3 in murine hematopoietic cell lines. J Biol Chem (1988) 2.19
Targets for global tuberculosis control. Int J Tuberc Lung Dis (2006) 2.16
The value of endoscopic treatment for ureteroceles during the neonatal period. J Urol (1998) 2.13
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment. J Med Genet (2005) 2.11
Isolation of cDNA and genomic clones encoding human pro-alpha 1 (III) collagen. Partial characterization of the 3' end region of the gene. J Biol Chem (1985) 2.09
[A case for diagnosis: scleroatrophic lichen of the glans]. Ann Dermatol Venereol (1992) 2.02
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling. Lancet (1999) 2.00
Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridization. Am J Hum Genet (1982) 1.98
Third consensus on medical treatment of metastatic breast cancer. Ann Oncol (2009) 1.96
Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome. Hum Genet (1986) 1.92
Nosocomial Legionnaires' disease caused by aerosolized tap water from respiratory devices. J Infect Dis (1982) 1.81
Human type I procollagen genes are located on different chromosomes. Proc Natl Acad Sci U S A (1982) 1.78
Systematic screening for active tuberculosis: rationale, definitions and key considerations. Int J Tuberc Lung Dis (2013) 1.70
In vivo kinetics of mRNA splicing and transport in mammalian cells. Mol Cell Biol (2002) 1.63
Connexin 26 gene linked to a dominant deafness. Nature (1998) 1.62
Regulation of gluconeogenesis at phosphoenolpyruvate carboxykinase. Curr Top Cell Regul (1984) 1.59
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1. Hum Mol Genet (1997) 1.59
[Outcome of children with repaired oesophageal atresia]. Arch Pediatr (2008) 1.59
Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19. Hum Genet (1985) 1.53
Determinants of disease in the simian immunodeficiency virus-infected rhesus macaque: characterizing animals with low antibody responses and rapid progression. J Gen Virol (1998) 1.51
Penetration of gentamicin. Administered intramuscularly and subconjunctivally into aqueous humor. Arch Ophthalmol (1969) 1.48
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum Mol Genet (1999) 1.44
[Endoscopic diagnosis of a gastric heterotopic pancreas and esophageal atresia: an incidental association?]. Arch Pediatr (2001) 1.44
Endemic and epidemic aspergillosis associated with in-hospital replication of Aspergillus organisms. J Infect Dis (1991) 1.38
[Accidental ingestion of caustics in children. Apropos of 100 cases]. Arch Fr Pediatr (1989) 1.38
Second consensus on medical treatment of metastatic breast cancer. Ann Oncol (2006) 1.37
[Necrotizing enterocolitis in two infants with gastroschisis]. Arch Pediatr (2008) 1.37
Carbohydrate and energy-yielding metabolism in non-conventional yeasts. FEMS Microbiol Rev (2000) 1.31
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2. Am J Hum Genet (1984) 1.30
GW body disassembly triggered by siRNAs independently of their silencing activity. Nucleic Acids Res (2007) 1.29
Unusual variation of the arterial pattern of the human upper limb. Anat Rec (1986) 1.28
Delta5-androstenediol is a natural hormone with androgenic activity in human prostate cancer cells. Proc Natl Acad Sci U S A (1998) 1.27
Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins. Am J Hum Genet (1997) 1.26
Cell lineage study in the liver using retroviral mediated gene transfer. Evidence against the streaming of hepatocytes in normal liver. Am J Pathol (1994) 1.24
Organization of the human pro-alpha 2(I) collagen gene. J Biol Chem (1987) 1.24
Human cellular fibronectin: comparison of the carboxyl-terminal portion with rat identifies primary structural domains separated by hypervariable regions. Biochemistry (1985) 1.23
Acute liver failure in infancy: a 14-year experience of a pediatric liver transplantation center. J Pediatr (2001) 1.22
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11. Clin Genet (2008) 1.21
Cloning and analysis of the 5' portion of the human type-III procollagen gene (COL3A1). Gene (1989) 1.21
[Liver hernia. Prognosis and report of 11 cases]. J Gynecol Obstet Biol Reprod (Paris) (2007) 1.20
The structural gene for aldolase B (ALDB) maps to 9q13----32. Ann Hum Genet (1985) 1.19
A specific promoter of the sensory cells of the inner ear defined by transgenesis. Hum Mol Genet (2001) 1.19
Torsion of the gallbladder in children. J Pediatr Surg (1994) 1.17
Assignment of the gene for F-type phosphofructokinase to human chromosome 10 by somatic cell hybridization and specific immunoprecipitation. Ann Hum Genet (1980) 1.17
Prevalence and significance of Legionella pneumophila contamination of residential hot-tap water systems. J Infect Dis (1985) 1.14
Ehlers-Danlos syndrome type IV: cosegregation of the phenotype to a COL3A1 allele of type III procollagen. Hum Genet (1986) 1.14
Postpneumonectomy syndrome in children: advantages and long-term follow-up of expandable prosthesis. J Pediatr Surg (2001) 1.14
[A rare case of epigastric heteropagus twinning]. J Gynecol Obstet Biol Reprod (Paris) (2001) 1.14
Congenital portosystemic shunts in children: recognition, evaluation, and management. Semin Liver Dis (2013) 1.14
Influence of antibiotics and cyclic polyethers on ion transport in mitochondria. Fed Proc (1969) 1.13
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB. Hum Mol Genet (1997) 1.13
Simian homologues of human gamma-2 and betaherpesviruses in mandrill and drill monkeys. J Virol (2000) 1.11
Activation of beta-catenin in epithelial and mesenchymal hepatoblastomas. Oncogene (2000) 1.11
Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance. Am J Hum Genet (1999) 1.10
Physiologic variations of the internal jugular vein surface, role of the omohyoid muscle, a preliminary echographic study. Surg Radiol Anat (1988) 1.10
Treatment of thyroid associated ophthalmopathy with periocular injections of triamcinolone. Br J Ophthalmol (2004) 1.10
Further evidence for the dispersion of the human fibrillar collagen genes. Am J Hum Genet (1986) 1.09
Phylogeny of Pneumocystis carinii from 18 primate species confirms host specificity and suggests coevolution. J Clin Microbiol (2001) 1.08
Tracheobronchial ruptures from blunt thoracic trauma in children. J Pediatr Surg (1999) 1.07
In vivo cooperation between introns during pre-mRNA processing. Genes Dev (1993) 1.06
Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females. Hum Mol Genet (1997) 1.05
The pro alpha 2(V) collagen gene is evolutionarily related to the major fibrillar-forming collagens. Nucleic Acids Res (1987) 1.04
Programmatic approaches to screening for active tuberculosis. Int J Tuberc Lung Dis (2013) 1.04
Isolation and characterization of the human fibrillar collagen genes. Ann N Y Acad Sci (1985) 1.02
[Localization of the gene for human acid alpha-glucosidase (alpha-GLUa) on the 17q21 to 17qter by interspecific hybridization (author's transl)]. Hum Genet (1979) 1.02
Outbreak of JK diphtheroid infections associated with environmental contamination. J Clin Microbiol (1984) 1.01
Analysis of the promoter region and the N-propeptide domain of the human pro alpha 2(I) collagen gene. Nucleic Acids Res (1985) 1.01
Outcomes and fate of the remnant moiety following laparoscopic heminephrectomy for duplex kidney: a multicenter review. J Pediatr Urol (2011) 1.01
Antibiotic inhibitors of mitochondrial ATP synthesis. Fed Proc (1975) 1.00
Tuberculosis and poverty: what is being done. Int J Tuberc Lung Dis (2011) 0.98
Long-term outcome of laparoscopic Nissen-Rossetti fundoplication for neurologically impaired and normal children. Surg Endosc (2007) 0.96
[Is procalcitonin able to help in pediatric appendicitis diagnosis?]. Ann Chir (2005) 0.96
Accumulation of mature mRNA in the nuclear fraction of mammalian cells. FEBS Lett (1999) 0.96
Comparative hemodynamic depression of sevoflurane versus halothane in infants: an echocardiographic study. Anesthesiology (1997) 0.95
Laparoscopic adrenalectomy in children. Surg Endosc (2001) 0.93
Human nidogen: cDNA cloning, cellular expression, and mapping of the gene to chromosome Iq43. Am J Hum Genet (1989) 0.93
[Localization of the gene for ribulose-5-phosphate-3-epimerase on the 2q32 to 2qter segment by interspecies cellular hybridization]. Ann Genet (1982) 0.93
[Assignment of the creatine kinase BB gene to chromosome 14 by man-rodent cell hybridization (author's transl)]. Ann Genet (1980) 0.93
Lymphoedema-area-restricted Sweet syndrome during G-CSF treatment. Lancet (1996) 0.92
Prevalence and molecular analysis of two hot spots for ectopic recombination leading to XX maleness. Genomics (1995) 0.92
A study of chromosomal changes associated with amplified dihydrofolate reductase genes in rat hepatoma cells and their dedifferentiated variants. J Cell Biol (1984) 0.92
Survival, proliferation, and functions of porcine hepatocytes encapsulated in coated alginate beads: a step toward a reliable bioartificial liver. Transplantation (1997) 0.92
Falling among the sensorially impaired elderly. Arch Phys Med Rehabil (1990) 0.91
Postnatal development of myenteric neurochemical phenotype and impact on neuromuscular transmission in the rat colon. Am J Physiol Gastrointest Liver Physiol (2010) 0.90
[Acquired non hypertrophic pyloric stenosis in children]. Arch Pediatr (2006) 0.90
Hep27, a member of the short-chain dehydrogenase/reductase family, is an NADPH-dependent dicarbonyl reductase expressed in vascular endothelial tissue. Cell Mol Life Sci (2006) 0.90
Radiological anatomy of the bile ducts based on intraoperative investigation in 250 cases. Anat Clin (1985) 0.90
The pro alpha 2(V) collagen gene (COL5A2) maps to 2q14----2q32, syntenic to the pro alpha 1 (III) collagen locus (COL3A1). Hum Genet (1986) 0.90
A series of vectors to construct lacZ fusions for the study of gene expression in Schizosaccharomyces pombe. FEBS Lett (1997) 0.89
Functional analysis of a dominant mutation of human connexin26 associated with nonsyndromic deafness. Cell Commun Adhes (2001) 0.88
[Localization of the LDHA-GST3-ESA4 synthetic group on human chromosome 11. Analyses of the classic man-rodent hybrids and of a new type (not adhering to the wall)]. Ann Genet (1983) 0.88
[Regional localization of the genes for human IDHs, MDHs PGK, alphaGAL, G6PD by interspecific hybridization (author's transl)]. Hum Genet (1977) 0.88
Multicentre phase II study of oxaliplatin as a single-agent in cisplatin/carboplatin +/- taxane-pretreated ovarian cancer patients. Ann Oncol (2002) 0.88
Chagas' myocarditis imported into France. Lancet (1988) 0.88
Regulation of pre-mRNA processing by src. Curr Biol (1995) 0.88