The 'Motorik-Modul' (MoMo): physical fitness and physical activity in German children and adolescents.

abstract：:Soon after birth a 36-week-gestational age, appropriate for dates, newborn infant developed hyperinsulinaemic hypoglycaemia which responded to diazoxide and glucose infusion. While normoglycaemic, he became increasingly ill with high lactate, pyruvate, and alanine levels. Provocation tests suggested a defect in lactat...

journal_title：European journal of pediatrics

authors： Aynsley-Green A,Weindling AM,Soltész G,Jenkins PA

更新日期：1983-12-01 00:00:00

abstract：UNLABELLED:The true burden of influenza in children is difficult to assess and is probably underestimated as clinical signs are usually nonspecific, and formal viral identification is rarely searched. In this study, we compare the clinical features of infections related to the new H1N1/09 influenza virus with infection...

journal_title：European journal of pediatrics

authors： Crisinel PA,Barazzone C,Kaiser L,L'Huillier AG,Taguebue J,Wagner N,Delcò C,Siegrist CA,Posfay-Barbe KM,H1N1 Pediatric Epidemiology Study Group.

更新日期：2012-01-01 00:00:00

abstract：:Mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria is associated with mutations in SUCLA2, the gene encoding a beta subunit of succinate-CoA ligase, where 17 patients have been reported. Mutations in SUCLG1, encoding the alpha subunit of the enzyme, have been reported in only one family,...

journal_title：European journal of pediatrics

authors： Ostergaard E,Schwartz M,Batbayli M,Christensen E,Hjalmarson O,Kollberg G,Holme E

更新日期：2010-02-01 00:00:00

abstract：UNLABELLED:In a national prospective study of risk factors for mother-to-child transmission of human immunodeficiency virus (HIV), 316 children of HIV-positive mothers were followed up for at least 6 months. Infection status was determined in 254 of them and 46 were found to be infected giving a transmission rate of 18...

journal_title：European journal of pediatrics

authors： Kind C

更新日期：1995-07-01 00:00:00

abstract：UNLABELLED:To date, the genetic basis of Dubowitz syndrome (short stature, microcephaly, facial abnormalities, eczema) is unknown and vascular complications are not known to be associated with this syndrome. In microcephalic osteodysplastic primordial dwarfism type II (MOPD II; disproportionate short statue, microcepha...

journal_title：European journal of pediatrics

authors： Dieks JK,Baumer A,Wilichowski E,Rauch A,Sigler M

更新日期：2014-09-01 00:00:00

abstract：:Since immunological disorders have been demonstrated in patients with Diamond-Blackfan anaemia (DBA), intravenous immunoglobulins (IVIG) were administered to a 14-year-old girl with DBA and congenital malformations, previously treated with corticosteroids and blood transfusions. No therapeutic effect was observed. ...

journal_title：European journal of pediatrics

authors： Miceli Sopo S,Pesaresi MA,Pastore M,Stabile A

更新日期：1990-08-01 00:00:00

abstract：:Small for gestational age (SGA) infants are known to develop relatively mild transient hyperbilirubinaemia, especially in comparison with premature infants. This may be interpreted as an index of accelerated maturation of particular vital functions. In the present study 12 SGA infants, 12 appropriate for gestational a...

journal_title：European journal of pediatrics

authors： von Stockhausen HB,Struve M

更新日期：1979-11-01 00:00:00

abstract：:We studied the clinical features, laboratory and thyroid functions and thyrotropin (TSH)-receptor and thyroid-stimulation antibodies in 21 patients with atrophic auto-immune thyroiditis (AAT) and 48 patients with goitrous auto-immune thyroiditis (GAT) of childhood onset. The clinical features of patient with AAT were ...

journal_title：European journal of pediatrics

authors： Matsuura N,Konishi J,Yuri K,Harada S,Fujieda K,Nohara Y,Mikami Y,Kasagi K,Iida Y,Hosoda A

更新日期：1990-05-01 00:00:00

abstract：:Human metapneumovirus (hMPV) is a recently discovered pathogen in respiratory tract infection. The published literature suggests milder illness severity in hMPV compared with respiratory syncytial virus (RSV) infection. In two consecutive seasons, 637 nasopharyngeal aspirates from pediatric patients were tested by hMP...

journal_title：European journal of pediatrics

authors： Wilkesmann A,Schildgen O,Eis-Hübinger AM,Geikowski T,Glatzel T,Lentze MJ,Bode U,Simon A

更新日期：2006-07-01 00:00:00

abstract：:Three sibs with an inherited form of male pseudohermaphroditism are described. They were all born with ambiguous external genitalia but no diagnosis of a possible enzyme defect was made during childhood. First seen at the ages of 16, 14 and 10 years respectively, they were investigated in order to establish the pathog...

journal_title：European journal of pediatrics

authors： Ivarsson SA,Nielsen MD,Lindberg T

更新日期：1988-06-01 00:00:00

abstract：:Chronic lung disease of prematurity (CLD) is a common respiratory disorder of preterm infants. At autopsy, fibroblast proliferation, and components of the extracellular matrix, including collagen and fibronectin, are markedly increased in the lungs of infants who die from CLD. Examination of broncho-alveolar fluid sug...

journal_title：European journal of pediatrics

authors： Kotecha S

更新日期：1996-08-01 00:00:00

abstract：:A 4-year-old boy is described with abdominal pain, emesis, weight loss, hypoproteinemia and edema. The diagnosis of Menetrier disease was made based on radiographic studies, gastroscopy and gastric biopsy. There was little response to medical treatment and enteral feedings were poorly tolerated for many weeks. Althoug...

journal_title：European journal of pediatrics

authors： Ling LJ,Hershenson MB,Young S,Traisman HS

更新日期：1986-02-01 00:00:00

abstract：:Achondroplasia, the most common form of chondrodysplasia, has been associated with mutations in the gene of the fibroblast growth factor receptor-3 (FGFR-3) on chromosome 4p. All 39 achondroplasia alleles studied so far carried point mutations which caused the same amino acid exchange, a substitution of glycine by arg...

journal_title：European journal of pediatrics

authors： Superti-Furga A,Eich G,Bucher HU,Wisser J,Giedion A,Gitzelmann R,Steinmann B

更新日期：1995-03-01 00:00:00

abstract：:Term born infants are predisposed to human rhinovirus (HRV) lower respiratory tract infections (LRTI) by reduced neonatal lung function and genetic susceptibility. Our aim was to investigate whether prematurely born infants were similarly predisposed to HRV LRTIs or any other viral LRTIs. Infants born less than 36 wee...

journal_title：European journal of pediatrics

authors： Drysdale SB,Alcazar M,Wilson T,Smith M,Zuckerman M,Hodemaekers HM,Janssen R,Bont L,Johnston SL,Greenough A

更新日期：2016-12-01 00:00:00

abstract：:Type I collagen is the major component of bone matrix; circulating carboxyterminal propeptide of type I procollagen (P-I-CP) levels reflect type I collagen synthesis in tissues and may be an useful index to investigate bone metabolism. We measured P-I-CP by a new radioimmunoassay in 300 healthy children and adolescent...

journal_title：European journal of pediatrics

authors： Saggese G,Bertelloni S,Baroncelli GI,Di Nero G

更新日期：1992-10-01 00:00:00

abstract：:We describe here an infant with a large, solitary, fluid-filled lung cyst and hyperinflation of adjacent lung tissue in the same lobe. The combination of a fluid-filled cyst and ectatic emphysema in the same lobe suggests bronchial collapse and airway obstruction as a contributory mechanism for this unusual roentgenog...

journal_title：European journal of pediatrics

authors： Stevenson DK,Silverman FN,Churg AM,Shochat SJ

更新日期：1979-10-01 00:00:00

abstract：:Following ion-exchange chromatography and subsequent thin-layer chromatography, 3 peculiar oligosaccharide excretion patterns were distinguished in 3 patients with beta-galactosidase deficiency. Each patient differed clinically and it is proposed that this method may be of use in characterizing various forms of beta-g...

journal_title：European journal of pediatrics

authors： Sewell AC,Gehler J,Spranger J

更新日期：1980-05-01 00:00:00

abstract：UNLABELLED:The inherited ion channel disorders (channelopathies) are a group of disorders caused by mutations in genes encoding ion channels. Ion channel disorders can affect any tissue, but the majority affect skeletal muscle or the central nervous system. These disorders include skeletal muscle sodium channelopathies...

journal_title：European journal of pediatrics

authors： Surtees R

更新日期：2000-12-01 00:00:00

abstract：:Shwachman-Diamond syndrome (SDS) is an autosomal recessive disorder characterised by skeletal dysplasia, exocrine pancreatic insufficiency and bone marrow failure. Various other conditions, such as hepatopathy and failure to thrive have been associated with SDS. A retrospective study was conducted to describe mutation...

journal_title：European journal of pediatrics

authors： Schaballie H,Renard M,Vermylen C,Scheers I,Revencu N,Regal L,Cassiman D,Sevenants L,Hoffman I,Corveleyn A,Bordon V,Haerynck F,Allegaert K,De Boeck K,Roskams T,Boeckx N,Bossuyt X,Meyts I

更新日期：2013-05-01 00:00:00

abstract：:A 10-year-old boy with chyluria due to a congenital fistulous communication between the lymphatic system and the bladder is described. Chyluria can be parasitic or non-parasitic. Many causes of non-parasitic chyluria have been reported. Lymphography is the preoperative imaging procedure of choice since it demonstrates...

journal_title：European journal of pediatrics

authors： Stalens JP,Falk M,Howmann-Giles R,Roy LP

更新日期：1992-01-01 00:00:00

abstract：:A 4-month-old infant was admitted to the Pediatric Intensive Care Unit with Pneumococcal meningitis. A few hours after admission he developed intractable convulsions that could not be stopped with phenytoin, phenobarbitone and a continuous drip of diazepam. Thiopentone sodium anaesthesia was induced for 24 h terminati...

journal_title：European journal of pediatrics

authors： Goitein KJ,Mussaffi H,Melamed E

更新日期：1983-04-01 00:00:00

abstract：:Clinical, morphological, ultrastructural and immunological studies were performed in a case of congenital self-healing non-Langerhans cell histiocytosis. The patient showed several aspects that have not been published before: a large nodule in the vulvar region, vesiculobullous elements and pneumonia (asymptomatic). T...

journal_title：European journal of pediatrics

authors： Oranje AP,Vuzevski VD,de Groot R,Prins ME

更新日期：1988-10-01 00:00:00

abstract：:A 9-year-old girl presented with a red scaly rash confined to sun-exposed areas which started at 2 years of age and had the appearance of pellagra. Investigation of urinary tryptophan metabolites following an oral tryptophan load, showed increased excretion of kynurenine and kynurenic acid but reduced excretion of 3-h...

journal_title：European journal of pediatrics

authors： Clayton PT,Bridges NA,Atherton DJ,Milla PJ,Malone M,Bender DA

更新日期：1991-05-01 00:00:00

abstract：:Haemodynamic assessment during the transitional period in preterm infants is challenging. We aimed to describe the relationships between cerebral regional tissue oxygen saturation (CrSO2), perfusion index (PI), echocardiographic, and clinical parameters in extremely preterm infants in their first 72 h of life. Twenty ...

journal_title：European journal of pediatrics

authors： Janaillac M,Beausoleil TP,Barrington KJ,Raboisson MJ,Karam O,Dehaes M,Lapointe A

更新日期：2018-04-01 00:00:00

abstract：UNLABELLED:Extremely immature newborns develop a self-limiting normal anion gap metabolic acidosis in early life. This study examined the natural history of this acidosis in a population of infants of gestation less than 26 weeks in the first 14 days of life. The acidosis was maximal on day 4 with a mean base deficit o...

journal_title：European journal of pediatrics

authors： Bourchier D,Weston PJ

更新日期：2015-01-01 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：UNLABELLED:Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental disorder commonly prevalent in children worldwide including Thailand. However, there are very few studies thus far addressing risk factors for ASD in Thai children. This case-control study aims to investigate whether various risk factors es...

journal_title：European journal of pediatrics

authors： Khaiman C,Onnuam K,Photchanakaew S,Chonchaiya W,Suphapeetiporn K

更新日期：2015-10-01 00:00:00

abstract：:An Arab Moslem kindred is reported in which six abnormal male fetuses were born in three closely related sibships. They had amelia, malformed head and other severe skeletal and visceral malformations. The similarities and differences between the developmental and inherent characteristics found in our patients and in f...

journal_title：European journal of pediatrics

authors： Zimmer EZ,Taub E,Sova Y,Divon MY,Pery M,Peretz BA

更新日期：1985-11-01 00:00:00

abstract：:Most pediatric asthma guidelines offer evidence-based or best practice approaches to the management of asthma exacerbations but struggle with evidence-based approaches for severe acute asthma (SAA). We aimed to investigate current practices in children with SAA admitted to European pediatric intensive care units (PICU...

journal_title：European journal of pediatrics

authors： Boeschoten S,de Hoog M,Kneyber M,Merkus P,Boehmer A,Buysse C

更新日期：2020-03-01 00:00:00

abstract：UNLABELLED:The 6-min walk test is a simple and accurate method to measure functional exercise capacity in children. We provide smooth reference curves for the modified 6-min walk test in 696 healthy children and adolescents aged 4-19 years, enabling calculation of sex-, age-, and height-specific Z-scores. CONCLUSION:T...

journal_title：European journal of pediatrics

authors： Saraff V,Schneider J,Colleselli V,Ruepp M,Rauchenzauner M,Neururer S,Geiger R,Högler W

更新日期：2015-06-01 00:00:00