Severe tick-borne encephalitis following passive immunization.

abstract：UNLABELLED:A newborn boy was referred to our hospital because of hemolytic anemia and severe hyperbilirubinemia. Extensive investigations aimed at determining the cause of hemolysis was initiated at the time of admission and 3 months after blood transfusion. Notably, no intrinsic erythrocyte abnormalities could be dete...

journal_title：European journal of pediatrics

authors： Vos MJ,Martens D,van de Leur SJ,van Wijk R

更新日期：2014-12-01 00:00:00

abstract：:Following a description of the genetic aspects of the human histocompatibility antigens system HLA and its principle typing methods, this paper reviews the relationship between HLA antigens, transplantation immunology and certain diseases. In particular, the role of the lymphocyte-defined antigens of the HLA-D system ...

journal_title：European journal of pediatrics

authors： Passarge E,Valentine-Thon E

更新日期：1980-03-01 00:00:00

abstract：:The objective of this study was to investigate the clinical applicability of pulse oximetry to measure haemoglobin oxygen saturation and heart rate in the first 20 min of life and to analyse the effect of pre- or post-ductal (hand, respectively, foot) fixation of sensors on oxygen saturation. Measurements were carried...

journal_title：European journal of pediatrics

authors： Meier-Stauss P,Bucher HU,Hürlimann R,König V,Huch R

更新日期：1990-09-01 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：:Of all newborn infants, 5% require some degree of basic life support at birth. Newborn resuscitation therefore is one of the most frequent procedures carried out in medicine. It is therefore important that the routines in use are evidence based. Newborn resuscitation can be divided into ten steps: (1) initial stabilis...

journal_title：European journal of pediatrics

authors： Saugstad OD

更新日期：1998-01-01 00:00:00

abstract：:In order to determine the hepatotoxicity of rifampicin in children treated for tuberculosis, a survey was performed of 18 children receiving this medicine in combination with isoniazid. Fifteen of the 18 children (83%) showed a rise in ASAT values and 11 (61%) in ALAT values exceeding 29U/L. Seven children with maxima...

journal_title：European journal of pediatrics

authors： Linna O,Uhari M

更新日期：1980-09-01 00:00:00

abstract：:Eight patients with the syndrome of benign paroxysmal vertigo of childhood are presented. This symptom complex is characterized by attacks of vertigo in young children combined with nystagmus, ataxia and transiently decreased vestibular function, but without impaired consciousness. Diagnostic and follow-up studies rev...

journal_title：European journal of pediatrics

authors： Koehler B

更新日期：1980-08-01 00:00:00

abstract：UNLABELLED:Familial Mediterranean fever (FMF) is characterised by recurrent fever and serositis. The most important complication of the disease is amyloidosis. Cheap and non-invasive methods would be important in predicting or establishing the early diagnosis of amyloidosis. For this purpose, we studied the role of uri...

journal_title：European journal of pediatrics

authors： Baskin E,Saatçi U,Ciliv G,Bakkaloglu A,Besbas N,Topaloglu R,Ozen S

更新日期：2003-05-01 00:00:00

abstract：UNLABELLED:Five neonates who suffered from an unexpected long period of respiratory failure, muscular hypotonia, and drowsiness were observed in a retrospective study. Prior to this general depression, unusually high doses of diazepam were administered to all patients via intravenous bolus injection. Serum levels of di...

journal_title：European journal of pediatrics

authors： Peinemann F,Daldrup T

更新日期：2001-06-01 00:00:00

abstract：:One year's experience in screening for congenital hypothyroidism in Greece is reported. Thyroid stimulating hormone (TSH) determination by a radioimmunoassay on dried blood spots was selected as the screening method. During the first year of screening 75,879 newborn infants were tested from Guthrie blood spots taken o...

journal_title：European journal of pediatrics

authors： Mengreli C,Kassiou K,Tsagaraki S,Pantelakis S

更新日期：1981-10-01 00:00:00

abstract：:The calorie intake and weight gain of 24 low birth weight (LBW) infants, less than 33 weeks gestation and less than 1500 g birth weight, was studied prospectively. Fourteen infants were fed on a commercially available LBW formula milk and ten were fed on their own mother's fresh unpasteurised expressed breast milk (EB...

journal_title：European journal of pediatrics

authors： Hendrickse WA,Spencer SA,Roberton DM,Hull D

更新日期：1984-11-01 00:00:00

abstract：: ...

journal_title：European journal of pediatrics

authors： Doudin A,Becker A,Rothenberger A,Meyer T

更新日期：2018-11-01 00:00:00

abstract：:The Kabuki (Niikawa-Kuroki) syndrome was reported in 1981 by Niikawa et al. and Kuroki et al. in a total of ten unrelated Japanese children with a characteristic array of multiple congenital anomalies and mental retardation. The syndrome is characterized by a distinct face, mild to moderate mental retardation, postnat...

journal_title：European journal of pediatrics

authors： Schrander-Stumpel C,Meinecke P,Wilson G,Gillessen-Kaesbach G,Tinschert S,König R,Philip N,Rizzo R,Schrander J,Pfeiffer L

更新日期：1994-06-01 00:00:00

abstract：UNLABELLED:Overweight and obesity are major public health issues. Childhood obesity often persists throughout adulthood. Recently a higher prevalence of obesity in adults whose mothers smoked during pregnancy was reported. The aim of this study was to assess whether this association is also detectable in pre-school chi...

journal_title：European journal of pediatrics

authors： Toschke AM,Koletzko B,Slikker W Jr,Hermann M,von Kries R

更新日期：2002-08-01 00:00:00

abstract：:Two regimens of steroid treatment for the initial attack of idiopathic nephrotic syndrome (NS) in children were compared in a controlled prospective multi-centre study. Long prednisone therapy consisted of 60 mg/m2 per 24 h for 6 weeks, followed by alternate day 40 mg/m2 per 48 h for 6 weeks. The standard prednisone t...

journal_title：European journal of pediatrics

authors： Ehrich JH,Brodehl J

更新日期：1993-04-01 00:00:00

abstract：:Pulmonary arterial hypertension is characterised by the presence of pulmonary hypertension (mean pulmonary artery pressure >25 mmHg at rest or >30 mmHg during exercise ) and normal pulmonary wedge pressure (<12 mmHg). Several risk factors for pulmonary arterial hypertension have been described. In the absence of any f...

journal_title：European journal of pediatrics

authors： Humbert M,Labrune P,Simonneau G

更新日期：2002-10-01 00:00:00

abstract：:An autosomal dominant hereditary bone dysplasia was observed in three members of a Sardinian family living in Germany--the father and two sons. The guiding clinical symptom is thickening of the wrist proximal to the styloid process of the ulna. The radiologically recognizable changes--non-calcified cartilaginous islan...

journal_title：European journal of pediatrics

authors： Rosenberg E,Löhr H

更新日期：1986-04-01 00:00:00

abstract：:Piritramide is indicated for treatment of postoperative pain and analgosedation in the intensive care unit (ICU) setting. In an open prospective study the pharmacokinetics of piritramide were investigated in four groups: newborns (NB, age: 1-28 days) (n=8), infants 1 (IF1, age: 2-4 months) (n=7), infants 2 (IF2, age: ...

journal_title：European journal of pediatrics

authors： Müller C,Kremer W,Harlfinger S,Doroshyenko O,Jetter A,Hering F,Hünseler C,Roth B,Theisohn M

更新日期：2006-04-01 00:00:00

abstract：UNLABELLED:The phenotypes of chromosomal 22q11.2 microdeletion are quite variable among individuals and hypoparathyroidism (HP) constitutes a definite portion of the clinical spectrum. For the correct diagnosis and pertinent follow up of the HP children due to del22q11.2, we tried to delineate the clinical characterist...

journal_title：European journal of pediatrics

authors： Adachi M,Tachibana K,Masuno M,Makita Y,Maesaka H,Okada T,Hizukuri K,Imaizumi K,Kuroki Y,Kurahashi H,Suwa S

更新日期：1998-01-01 00:00:00

abstract：:The urofacial syndrome is a rare condition that occurs in both genders and characterized by uropathy and facial abnormalities. Early diagnosis is crucial for the management and prognosis of urinary problems. Paradoxical inversion of facial musculature when smiling, giving an appearance of crying associated with severe...

journal_title：European journal of pediatrics

authors： Mermerkaya M,Süer E,Öztürk E,Gülpınar Ö,Gökçe Mİ,Yalçındağ FN,Soygür T,Burgu B

更新日期：2014-05-01 00:00:00

abstract：:Although thyroid medications are frequently prescribed during pregnancy, paediatricians treating the respective neonates often have no information about the underlying maternal thyroid disease, and inconsistencies in postnatal diagnostics may result. We analysed a cohort of 1819 mothers admitted for delivery in 1 year...

journal_title：European journal of pediatrics

authors： Weissenfels PC,Woelfle J,Korsch E,Joergens M,Gohlke B

更新日期：2018-11-01 00:00:00

abstract：:Lung ultrasound (LUS) has been described as a useful tool in early prognosis of several respiratory diseases of the newborn, especially preterm infant newborns (PTNB) with respiratory distress syndrome (RDS), but still, it is not a standard of care in many neonatal units. We have conducted a descriptive, prospective s...

journal_title：European journal of pediatrics

authors： Gregorio-Hernández R,Arriaga-Redondo M,Pérez-Pérez A,Ramos-Navarro C,Sánchez-Luna M

更新日期：2020-01-01 00:00:00

abstract：:Histochemical and immunohistochemical studies performed in only a few cases of sinus histiocytosis with massive lymphoadenopathy (SHML) indicated that SHML cells belong to the macrophage--histiocyte system, though their exact origin is still uncertain. We analyzed the morphological, antigenic and enzymatic characteris...

journal_title：European journal of pediatrics

authors： Paulli M,Locatelli F,Kindl S,Boveri E,Facchetti F,Porta F,Rosso R,Nespoli L,Magrini U

更新日期：1992-09-01 00:00:00

abstract：UNLABELLED:Desmopressin (DDAVP) is frequently used in the treatment of primary isolated enuresis nocturna if other approaches have failed. We report a further case of hyponatraemia and cerebral convulsion due to water intoxication after intranasal DDAVP application by a 6 year-old boy with enuresis. CONCLUSION:Althoug...

journal_title：European journal of pediatrics

authors： Schwab M,Wenzel D,Ruder H

更新日期：1996-01-01 00:00:00

abstract：:A 17-year-old patient suffering from Crohn disease (CD) and liver cirrhosis is presented. At an advanced stage of the disease, he died of a concomitant urosepsis. Autopsy showed that the liver cirrhosis was caused by sclerosing cholangitis. This very rare complication of CD in adolescence is discussed. ...

journal_title：European journal of pediatrics

authors： Ramelli GP,Tönz O,Zimmermann A,Lentze MJ

更新日期：1991-06-01 00:00:00

abstract：:Despite neonatal lung ultrasound (LU) being diffused worldwide, its introduction in limited-resource areas has not been formally investigated. We conceived a project to introduce it in a level 3 NICU of a developing country and verify if, after a short protocolized training, clinicians may efficaciously use LU. Inter-...

journal_title：European journal of pediatrics

authors： Mazmanyan P,Kerobyan V,Shankar-Aguilera S,Yousef N,De Luca D

更新日期：2020-07-01 00:00:00

abstract：:The aim of this study is to evaluate and compare mothers' and grandparents' feeding behaviours, the differences between the behaviours, the relationship between children's feeding problems and grandparents' feeding behaviours, as well as the relationship between grandparents' feeding behaviour and children's body mass...

journal_title：European journal of pediatrics

authors： Metbulut AP,Özmert EN,Teksam O,Yurdakök K

更新日期：2018-12-01 00:00:00

abstract：UNLABELLED:Cleidocranial dysplasia (CCD; MIM 119600) is an autosomal dominant skeletal dysplasia characterised by hypoplastic clavicles, patent fontanelles, short stature, tooth anomalies and other variable skeletal changes. Different mutations of the RUNX2/CBFA1 gene (MIM 600211) have been detected in patients with CC...

journal_title：European journal of pediatrics

authors： Morava E,Kárteszi J,Weisenbach J,Caliebe A,Mundlos S,Méhes K

更新日期：2002-11-01 00:00:00

abstract：:Haemostasis was studied in 8 tall girls during treatment with high doses of synthetic oestrogens for a period of 1 to 28 months. The girls received 0.5 mg ethinyloestradiol daily from day 1 to day 25 and 15 mg norethisteron daily from day 21 to day 25. All were without clinical signs of thromboembolism. Factors of the...

journal_title：European journal of pediatrics

authors： Muntean W,Borkenstein M

更新日期：1980-09-01 00:00:00

abstract：:Serum IgE concentration was measured on the 5th day of life in 943 infants. All infants were included in a 3 month follow-up study. The frequency of cow's milk allergy was studied according to either family history, IgE level, or both. Feeding (mother's milk or formula feeding) was taken into account. Manifestations s...

journal_title：European journal of pediatrics

authors： Vandenplas Y,Sacre L

更新日期：1986-12-01 00:00:00