Ipratropium bromide for symptomatic preterm infants.

abstract：UNLABELLED:Both news media and entertainment fiction may lead to short-term and enduring fright reactions. Even TV programs, movies and news made for children may trigger fear. Preoperational children (3 to 7 years of age) are most afraid of fantasy characters, transformations and interpersonal violence. Operational ch...

journal_title：European journal of pediatrics

authors： Custers K,Van den Bulck J

更新日期：2012-04-01 00:00:00

abstract：:Twenty-six children with cerebral palsy were examined with respect to structural asymmetry of the mouth. In 19 children there were clear cut correlations between symmetry/asymmetry of voluntary function and the oral findings. Patients with symmetrical patterns of movements had symmetrical dentition, while in those wit...

journal_title：European journal of pediatrics

authors： Haberfellner H,Richter M

更新日期：1980-12-01 00:00:00

abstract：:Beckwith-Wiedemann syndrome is an overgrowth disorder characterized by neonatal macrosomia, abdominal wall defects, macroglossia, renal anomalies, organomegaly, hypoglycemia, and cancer predisposition. Hepatoblastoma is the second most frequent tumor and periodic serum alpha-fetoprotein (αFP) dosage is the cornerstone...

journal_title：European journal of pediatrics

authors： Mussa A,Ferrero GB,Ceoloni B,Basso E,Chiesa N,De Crescenzo A,Pepe E,Silengo M,de Sanctis L

更新日期：2011-11-01 00:00:00

abstract：:Two children with congenital cytomegalovirus infection and intracerebral echogenicities were investigated by computer sonography and colour Doppler imaging (CDI). By simultaneous imaging of brain tissue and CDI, blood flow within the stripe-like echogenicities of the basal ganglia was demonstrated. Using CDI the echog...

journal_title：European journal of pediatrics

authors： Ries M,Deeg KH,Heininger U

更新日期：1990-11-01 00:00:00

abstract：:Dyggve-Melchior-Clausen (DMC) syndrome is a rare autosomal recessive disorder characterized by the association of a progressive spondyloepimetaphyseal dysplasia and mental retardation ranging from mild to severe. The disorder results from mutations in the dymeclin (DYM) gene in the 18q12-12.1 chromosomal region. We re...

journal_title：European journal of pediatrics

authors： Khalifa O,Imtiaz F,Al-Sakati N,Al-Manea K,Verloes A,Al-Owain M

更新日期：2011-01-01 00:00:00

abstract：:Clinically visible corneal opacities were observed in a patient with an extremely severe form of mucopolysaccharidosis II. In a second patient with an unusually mild form of mucopolysaccharidosis II, discrete corneal opacities were detected by slit-lamp examination. Thus clear corneae can no longer be regarded as a ha...

journal_title：European journal of pediatrics

authors： Spranger J,Cantz M,Gehler J,Liebaers I,Theiss W

更新日期：1978-08-17 00:00:00

abstract：:This study assessed the agreement between arterial and venous blood lactate and pH levels in children with sepsis. This retrospective, three-year study involved 60 PICU patients, with data collected from electronic or paper patient records. The inclusion criteria comprised of children (≤17 years old) with sepsis and t...

journal_title：European journal of pediatrics

authors： Samaraweera SA,Gibbons B,Gour A,Sedgwick P

更新日期：2017-08-01 00:00:00

abstract：:There has been some limited progress in the understanding of the basic defect in Wilson disease and the gene concerned has been located to the chromosome region 13q14. Treatment with zinc has emerged as a definite alternative to penicillamine administration and some shortcomings and/or hazards of both forms of therapy...

journal_title：European journal of pediatrics

authors： Danks DM

更新日期：1991-01-01 00:00:00

abstract：:In our clinic the decision on whether to continue with dietary treatment of phenylketonuria or not is left to each adolescent and adult patient after the advantages and disadvantages, as discussed in this paper, of continuing diet have been presented to them. As a result 61 of 132 patients have stopped diet or decline...

journal_title：European journal of pediatrics

authors： Brenton DP,Tarn AC,Cabrera-Abreu JC,Lilburn M

更新日期：1996-07-01 00:00:00

abstract：:Two young boys were referred for evaluation of metabolic myopathy because of elevated serum levels of creatine kinase, cramps and pigmenturia. Immunohistochemical studies of dystrophin in muscle biopsies showed reduced intensity of the stain with a patchy and discontinuous pattern in most fibers. In both patients dyst...

journal_title：European journal of pediatrics

authors： Minetti C,Tanji K,Chang HW,Medori R,Cordone G,DiMauro S,Bonilla E

更新日期：1993-10-01 00:00:00

abstract：:We report on a youngster followed by his paediatrician from birth until 14 years of age for premature beats, most likely of ventricular origin. The sudden death of his sister provoked a re-assessment of his electrocardiograms (ECG), resulting in the diagnosis of Brugada syndrome and the subsequent implantation of a ca...

journal_title：European journal of pediatrics

authors： Mivelaz Y,Di Bernardo S,Pruvot E,Meijboom EJ,Sekarski N

更新日期：2006-08-01 00:00:00

abstract：:Resting metabolic rate (RMR) and the thermic effect of a meal (TEM) were measured in a group of 26 prepubertal children divided into three groups: (1) children with both parents obese (n = 8, group OB2); (2) children with no obese parents and without familial history of obesity (n = 8, OB0); and (3) normal body weight...

journal_title：European journal of pediatrics

authors： Maffeis C,Schutz Y,Zoccante L,Pinelli L

更新日期：1993-02-01 00:00:00

abstract：UNLABELLED:The treatment of blunt splenic injuries (BSI) has undergone a significant shift away from an operative approach to a conservative treatment regimen in the last decades. Data concerning long-term follow-up of children sustaining BSI are largely confined to telephone surveys. Children treated with BSI over a 3...

journal_title：European journal of pediatrics

authors： Singer G,Rieder S,Eberl R,Wegmann H,Hoellwarth ME

更新日期：2013-09-01 00:00:00

abstract：:Seven male Japanese children with chronic granulomatous disease were given sulfamethoxazole-trimethoprim (SMX-TMP) for recurrent pyogenic infections, most of which had proved difficult to control with other antibiotics. With continous treatment the children remained free of infections severe enough to necessitate hosp...

journal_title：European journal of pediatrics

authors： Kobayashi Y,Amano D,Ueda K,Kagosaki Y,Usui T

更新日期：1978-04-20 00:00:00

abstract：UNLABELLED:Chronic lung disease (CLD) is an inflammatory disorder; in patients with other inflammatory disorders exhaled nitric oxide (NO) levels are elevated. The aim of this study was to test the hypothesis that prematurely born infants with CLD would have elevated exhaled NO levels compared to those without CLD and ...

journal_title：European journal of pediatrics

authors： Leipälä JA,Williams O,Sreekumar S,Cheeseman P,Rafferty GF,Hannam S,Milner A,Greenough A

更新日期：2004-09-01 00:00:00

abstract：:We aimed to assess the prevalence and outcomes of esophageal perforation in very low birth weight infants. This retrospective cohort study utilized the US National Inpatient Sample dataset for the years 2000 to 2017. A total of 1,755,418 very low birth weight infants were included; of them, 861 (0.05%) were diagnosed ...

journal_title：European journal of pediatrics

authors： Elgendy MM,Othman H,Aly H

更新日期：2021-02-01 00:00:00

abstract：UNLABELLED:The aim of this study was to provide growth and sexual maturation reference data for Turkish children living in The Netherlands. We also compared these references with the reference data of children of Dutch origin and with Turkish reference data collected in Turkey and elsewhere in Europe. Cross-sectional g...

journal_title：European journal of pediatrics

authors： Fredriks AM,van Buuren S,Jeurissen SE,Dekker FW,Verloove-Vanhorick SP,Wit JM

更新日期：2003-11-01 00:00:00

abstract：:Respiratory syncytial virus (RSV) infection is one of the main causes of infant hospitalization and mortality. The single-stranded RNA virus codes for 11 proteins of which the F protein, a surface epitope responsible for RSV fusion, is the most targeted for developing antiviral medicines and vaccines. The peak of symp...

journal_title：European journal of pediatrics

authors： Xing Y,Proesmans M

更新日期：2019-02-01 00:00:00

abstract：:It is rare that coloboma, heart anomalies, choanal atresia, retarded growth and development, and genital and ear anomalies (CHARGE) syndrome patients have DiGeorge sequence showing severe immunodeficiency due to the defect of the thymus. Although the only treatment to achieve immunological recovery for these patients ...

journal_title：European journal of pediatrics

authors： Inoue H,Takada H,Kusuda T,Goto T,Ochiai M,Kinjo T,Muneuchi J,Takahata Y,Takahashi N,Morio T,Kosaki K,Hara T

更新日期：2010-07-01 00:00:00

abstract：:To access outcome following hypoxic ischemic encephalopathy (HIE), survivors without cerebral palsy were invited for formal developmental assessment. Children aged ≥ 42 months were assessed using the NEPSY-2, Movement Assessment Battery for Children 2 (Movement ABC-2), Behavior Rating Inventory of Executive Function, ...

journal_title：European journal of pediatrics

authors： Hayes BC,Doherty E,Grehan A,Madigan C,McGarvey C,Mulvany S,Matthews TG,King MD

更新日期：2018-01-01 00:00:00

abstract：UNLABELLED:Sepsis is the major cause of morbidity and mortality in children, especially in immunocompromised patients, and a rapid identification of causative pathogen is strongly related with a better outcome. This prospective study analyzes the role of a multiplex real-time polymerase chain reaction in sepsis' etiolo...

journal_title：European journal of pediatrics

authors： Denina M,Scolfaro C,Colombo S,Calitri C,Garazzino S,Barbui Anna A,Brossa S,Regina Margherita Children’s Hospital Bloodstream Infections Study Group participants.,Tovo PA

更新日期：2016-08-01 00:00:00

abstract：UNLABELLED:Aim of our study was to evaluate Doppler renal blood flow velocity in asphyxiated neonates and to correlate renal function to Doppler findings. Doppler renal blood flow velocity was evaluated in 23 severely asphyxiated neonates born at a gestational age > 32 weeks and compared to our standard Doppler data ob...

journal_title：European journal of pediatrics

authors： Luciano R,Gallini F,Romagnoli C,Papacci P,Tortorolo G

更新日期：1998-08-01 00:00:00

abstract：UNLABELLED:We describe a case of iatrogenic pseudo-Bartter syndrome caused by administration of prostaglandin E1 (PGE1 alprostadil). Although the use of i.v. PGE1 is a well-established pharmacological therapy in neonates with a ductus-dependent congenital cardiopathy to ensure ductus-dependent flow, we could only find ...

journal_title：European journal of pediatrics

authors： Vanhaesebrouck S,Allegaert K,Vanhole C,Devlieger H,Gewillig M,Proesmans W

更新日期：2003-09-01 00:00:00

abstract：:This is a report on two mentally retarded sibs with similar anomalies (sagittal craniosynostosis, complex cardiovascular malformations, mandibular ankylosis) and various dysmorphic features. They could represent a "new" probably monogenic syndrome. ...

journal_title：European journal of pediatrics

authors： Pfeiffer RA,Singer H,Zschiesche S

更新日期：1987-01-01 00:00:00

abstract：:We report two Chinese boys with Wiskott-Aldrich syndrome presenting with gastro-intestinal bleeding, eczema and recurrent infection. They had thrombocytopenia and the mean platelet volume was small. Serum IgG and IgA were elevated and lymphocyte proliferation in response to phytohaemagglutinin, concanavalin A and poke...

journal_title：European journal of pediatrics

authors： Lau YL,Jones BM,Low LC,Wong SN,Leung NK

更新日期：1992-09-01 00:00:00

abstract：:An asthmatic child is presented who developed a cushingoid appearance with evidence of adrenal suppression and growth impairment while on low dose inhaled topical steroids. When the inhaled steroids were replaced by inhaled sodium cromoglycate his adrenal function recovered while his appearance and growth returned to ...

journal_title：European journal of pediatrics

authors： Priftis K,Everard ML,Milner AD

更新日期：1991-04-01 00:00:00

abstract：:Presentation of cystic fibrosis (CF) with an acrodermatitis enteropathica-like skin rash, anemia, and hypoproteinemia without pulmonary disease is rarely reported before. We describe an 11-month-old boy with rash and edema as the presenting signs of cystic fibrosis. The interesting additional finding in our patient wa...

journal_title：European journal of pediatrics

authors： Dalgic B,Egritas O

更新日期：2011-10-01 00:00:00

abstract：:Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder and the most disabling condition of heterotopic (extraskeletal) ossification in humans. Extraskeletal bone formation associated with inflammation preceding the osseous conversion usually begins in the first decade, predominantly in the head, neck, ...

journal_title：European journal of pediatrics

authors： Kartal-Kaess M,Shore EM,Xu M,Schwering L,Uhl M,Korinthenberg R,Niemeyer C,Kaplan FS,Lauten M

更新日期：2010-11-01 00:00:00

abstract：:We review the validity of balloon occlusion aortography (BOA) on the basis of our personal experience with 18 patients with congenital heart disease (mean weight 4.55 g, including 8 neonates). Four of the 18 patients underwent aortic arch angiography using balloon occlusion of the descending aorta. Pulmonary angiograp...

journal_title：European journal of pediatrics

authors： Ino T,Shimazaki S,Nishimoto K,Akimoto K,Iwahara M,Yabuta K,Watanabe M,Tanaka A,Hosoda Y

更新日期：1991-02-01 00:00:00

abstract：:Acute pharyngitis is one of the most frequent causes of primary care physician visits; however, there is no agreement about which is the best strategy to diagnose and manage acute pharyngitis in children. The aim of the current study was to evaluate the cost-effectiveness of the recommended strategies to diagnose and ...

journal_title：European journal of pediatrics

authors： Giraldez-Garcia C,Rubio B,Gallegos-Braun JF,Imaz I,Gonzalez-Enriquez J,Sarria-Santamera A

更新日期：2011-08-01 00:00:00