Heme oxygenase-1 expression in premature and mature neonates during the first week of life.

abstract：:The results of 24 h oesophageal pH monitoring, performed in 129 infants aged 6-10 weeks, were compared to those in the same patients after shorter periods (3, 6, 9 and 12 h). In the investigated population there was no significant difference between the reflux index (percentage of time with a pH < 4.0) after 12 or 24 ...

journal_title：European journal of pediatrics

authors： Vandenplas Y,Casteels A,Naert M,Derde MP,Blecker U

更新日期：1994-02-01 00:00:00

abstract：UNLABELLED:Melatonin is secreted during the night in adults but not in infants. It has a hypnotic effect as well as a relaxing effect on the smooth muscle of the gastrointestinal tract. It is plausible that breast milk, which consists of melatonin, may have an effect on improving infants' sleep and reducing infantile c...

journal_title：European journal of pediatrics

authors： Cohen Engler A,Hadash A,Shehadeh N,Pillar G

更新日期：2012-04-01 00:00:00

abstract：:A benign cystic nephroblastoma in a 6-month-old boy is presented. Erroneous interpretation as malignant nephroblastoma led to unnecessarily aggressive therapy. There is no evidence of recurrence or metastatic disease 12 years after the initial resection. As shown in our case and in the others previously reported in th...

journal_title：European journal of pediatrics

authors： Havers W,Stambolis C

更新日期：1979-05-18 00:00:00

abstract：:A 4-month-old male infant was seen because of an asymptomatic undescended left testis and a right sided abdominal mass. CT revealed a calcified retroperitoneal tumour. Histological examination of surgical specimens showed a mature primary teratoma of the contralateral undescended testis. While this is very rare, infan...

journal_title：European journal of pediatrics

authors： Azumagawa K,Mimaki T,Tanoue H,Mino M

更新日期：1993-11-01 00:00:00

abstract：:Triple A syndrome (TAS) or Allgrove syndrome (OMIM #231550) is a rare autosomal recessive disorder characterised by adrenocorticotropic hormone-resistant adrenal insufficiency, alacrima, achalasia, and neurological and dermatological abnormalities. Mutations in the AAAS gene on chromosome 12q13 encoding the nuclear po...

journal_title：European journal of pediatrics

authors： Kurnaz E,Duminuco P,Aycan Z,Savaş-Erdeve Ş,Muratoğlu Şahin N,Keskin M,Bayramoğlu E,Bonomi M,Çetinkaya S

更新日期：2018-03-01 00:00:00

abstract：:The internet is an integral tool for information, communication, and entertainment among adolescents. As adolescents devote increasing amounts of time to utilizing the internet, the risk for adopting excessive and pathological internet use is inherent. The study objectives include assessing the characteristics and pre...

journal_title：European journal of pediatrics

authors： Tsitsika A,Critselis E,Kormas G,Filippopoulou A,Tounissidou D,Freskou A,Spiliopoulou T,Louizou A,Konstantoulaki E,Kafetzis D

更新日期：2009-06-01 00:00:00

abstract：UNLABELLED:Rhizomelic chondrodysplasia punctata (RCDP) is clinically characterized by symmetrical shortening of the proximal limbs, contractures of joints, a characteristic dysmorphic face, and cataracts. In the classical form an impairment of several peroxisomal functions and enzymes (plasmalogen synthesis, phytanic a...

journal_title：European journal of pediatrics

authors： Hebestreit H,Wanders RJ,Schutgens RB,Espeel M,Kerckaert I,Roels F,Schmausser B,Schrod L,Marx A

更新日期：1996-12-01 00:00:00

abstract：UNLABELLED:Portal vein thrombosis is a rare but potentially lethal complication in children requiring splenectomy. We report on a 15-year-old boy with a dehydrated hereditary stomatocytosis, who underwent splenectomy and presented a postoperative partial portal vein thrombosis. With prompt heparin therapy, neither prop...

journal_title：European journal of pediatrics

authors： Perel Y,Dhermy D,Carrere A,Chateil JF,Bondonny JM,Micheau M,Barbier R

更新日期：1999-08-01 00:00:00

abstract：:Osteoporosis-pseudoglioma syndrome (OPPG) is a rare autosomal-recessive disorder, characterized by severe osteoporosis and early-onset blindness. Loss of function mutations in the gene encoding low-density lipoprotein receptor-related protein 5 (LRP5) have been established as the genetic defect of the disease. We repo...

journal_title：European journal of pediatrics

authors： Papadopoulos I,Bountouvi E,Attilakos A,Gole E,Dinopoulos A,Peppa M,Nikolaidou P,Papadopoulou A

更新日期：2019-03-01 00:00:00

abstract：:This randomized double-blind placebo-controlled trial evaluated the effects of early postnatal oral vitamin A supplementation (VAS) in 196 inborn very-low birth weight (VLBW) infants requiring respiratory support at 24 h of age. Eligible infants were randomized to receive aqueous syrup of vitamin A (10,000 IU of retin...

journal_title：European journal of pediatrics

authors： Basu S,Khanna P,Srivastava R,Kumar A

更新日期：2019-08-01 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：:Three infants with severe combined immunodeficiency and adenosine deaminase (ADA) deficiency were treated by T-cell depleted bone marrow transplantation (BMT), using human leukocyte antigen (HLA)-haploidentical parents as donors. In the first patient, two initial transplants failed to engraft and no change of the immu...

journal_title：European journal of pediatrics

authors： Bluetters-Sawatzki R,Friedrich W,Ebell W,Vetter U,Stoess H,Goldmann SF,Kleihauer E

更新日期：1989-11-01 00:00:00

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:Periventricular leucomalacia is a condition that causes lifelong disability and considerable economic burden. It occurs in premature infants of less than 32 weeks gestation due to their unique anatomical features. The white matter of these infants is poorly vascularised and contains oligodendrocyte progenito...

journal_title：European journal of pediatrics

authors： Blumenthal I

更新日期：2004-08-01 00:00:00

abstract：:In 41 preterm neonates with a gestational age (GA) varying from 27 to 36 weeks, glomerular filtration rate (GFR) was measured by means of the continuous inulin infusion technique. The reliability of the technique was confirmed. During postnatal development GFR was found to increase in two ways: firstly, an increase wi...

journal_title：European journal of pediatrics

authors： van der Heijden AJ,Grose WF,Ambagtsheer JJ,Provoost AP,Wolff ED,Sauer PJ

更新日期：1988-10-01 00:00:00

abstract：INTRODUCTION:Reduced concentrations of glucose-6-phospate dehydrogenase (G6PD) render erythrocytes susceptible to hemolysis under conditions of oxidative stress. In favism, the ingestion of fava beans induces an oxidative stress to erythrocytes, leading to acute hemolysis. DISCUSSION:The simultaneous occurrence of met...

journal_title：European journal of pediatrics

authors： Schuurman M,van Waardenburg D,Da Costa J,Niemarkt H,Leroy P

更新日期：2009-07-01 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：:The Dubowitz syndrome is a rare, autosomal, recessively inherited disorder of intrauterine and postnatal growth retardation leading to microcephaly, moderate mental retardation and such characteristic facial anomalies as telecanthus, epicanthic folds, blepharophimosis, ptosis, broadening of the bridge and tip of the n...

journal_title：European journal of pediatrics

authors： Küster W,Majewski F

更新日期：1986-04-01 00:00:00

abstract：:The glycogen storage disorders (GSD)-I, -III, -VI and -VIII are associated with hypertriglyceridaemia or mixed hyperlipidaemia which poses the question whether these patients have an increased risk for atherosclerosis. The atherogenicity of triglycerides has remained controversial, while increased plasma cholesterol l...

journal_title：European journal of pediatrics

authors： Schmitz G,Hohage H,Ullrich K

更新日期：1993-01-01 00:00:00

abstract：:In a five-year-old girl with congenital hepatic fibrosis raised erythrocyte sedimentation rate and serum gammaglobulins were noted for 3 years. Needle liver biopsy showed histological features of cholangitis and Klebsiella oxytoca was cultured from a liver biopsy specimen. Antibiotic treatment resulted in normalizatio...

journal_title：European journal of pediatrics

authors： Alvarez F,Hadchouel M,Bernard O

更新日期：1982-11-01 00:00:00

abstract：UNLABELLED:Growth hormone (GH) secretion was determined by evaluating circadian GH profiles for 24 h and GH responses to clonidine stimulation test and insulin-stimulated hypoglycaemia (ITT), in nine prepubertal children with beta-thalassaemia major (TM) and 17 with non-GH deficient short stature (NGHDSS). The TM child...

journal_title：European journal of pediatrics

authors： Katzos G,Harsoulis F,Papadopoulou M,Athanasiou M,Sava K

更新日期：1995-06-01 00:00:00

abstract：UNLABELLED:Isolated partial 3-methylcrotonyl-CoA carboxylase (MCC) deficiency has been described to be the cause for a distinct relatively mild clinical picture in a single patient. We describe another patient with isolated partial MCC deficiency who suffered from failure to thrive, muscular hypotonia and progressive r...

journal_title：European journal of pediatrics

authors： Wiesmann UN,Suormala T,Pfenninger J,Baumgartner ER

更新日期：1998-03-01 00:00:00

abstract：UNLABELLED:We investigated the histological and molecular characteristics of pulmonary alveolar proteinosis (PAP) in two siblings (a brother and sister) who did not exhibit respiratory distress at birth but who each developed symptoms during infancy. Histological analysis of lung specimens showed positive staining for ...

journal_title：European journal of pediatrics

authors： Sakai Y,Abo W,Yoshimura H,Sano H,Kuroki Y,Satoh M,Kaimori M

更新日期：1999-05-01 00:00:00

abstract：:To evaluate the feasibility and clinical usefulness of immunocytochemical detection of bone marrow metastases in neuroblastoma, we studied bone marrow samples from patients undergoing intensive therapy, followed in the majority of cases by autologous bone marrow rescue. Two monoclonal antibodies were used in an indire...

journal_title：European journal of pediatrics

authors： Beck D,Maritaz O,Gross N,Favrot M,Vultier N,Bailly C,Villa I,Gentilhomme O,Philip T

更新日期：1988-08-01 00:00:00

abstract：UNLABELLED:The aim of this study is to give a systematic overview on publications having investigated the allergy preventive effect of extensively and/or partially hydrolysed infant formulas. Publications were searched by several strategies. Inclusion criteria were: prospective cohort study, randomisation, family histo...

journal_title：European journal of pediatrics

authors： Schoetzau A,Gehring U,Wichmann HE

更新日期：2001-06-01 00:00:00

abstract：:The effects of intravenous injections of the opiate antagonist naloxone (0.005-0.4 mg/kg body weight) on respiratory pattern, apnoea duration and frequency were investigated in six infants with severe sleep apnoea syndrome. Since several authors found elevated plasma- and CSF-levels of endogenous opioids (endorphines)...

journal_title：European journal of pediatrics

authors： Haidmayer R,Kerbl R,Meyer U,Kerschhaggl P,Kurz R,Kenner T

更新日期：1986-10-01 00:00:00

abstract：:Clinical pharmacists provide beneficial services to adult patients, though their benefits for paediatric hospital patients are less defined. Five databases were searched using the MeSH terms 'clinical pharmacist', 'paediatric/paediatric', 'hospital', and 'intervention' for studies with paediatric patients conducted in...

journal_title：European journal of pediatrics

authors： Drovandi A,Robertson K,Tucker M,Robinson N,Perks S,Kairuz T

更新日期：2018-08-01 00:00:00

abstract：:Serum immunoreactive erythropoietin (siEPO) was determined in cord serum from neonates (n = 97, gestational age 36-43 weeks), in healthy children from birth to adolescence (n = 260) and in children with haematological (n = 30), renal (n = 10) and congenital heart diseases (n = 70). In healthy children siEPO levels dec...

journal_title：European journal of pediatrics

authors： Eckardt KU,Hartmann W,Vetter U,Pohlandt F,Burghardt R,Kurtz A

更新日期：1990-04-01 00:00:00

abstract：:The study was planned to determine identifiable starting points of a trend towards obesity and the influence of variables in preschool children aged 0 to 6 years. In this longitudinal follow-up study, 102 children were enrolled. Anthropometric measurements such as weight-height centiles (specific for gender and age gr...

journal_title：European journal of pediatrics

authors： Yücel O,Kinik ST,Aka S

更新日期：2011-06-01 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