Extent of fussing and colic type crying preceding atopic disease.

abstract：:Transient hyperphosphatasaemia is usually a chance finding arising from the use of biochemical screening profiles. Clinical correlates in cases so far described have been non-specific. ...

journal_title：Archives of disease in childhood

authors： Arthur LJ,Hill PG,Attenburrow AA

更新日期：1984-10-01 00:00:00

abstract：OBJECTIVE:To report the evidence for and challenges to the validity of Sheffield Peer Review Assessment Tool (SPRAT) with paediatric Specialist Registrars (SpRs) across the UK as part of Royal College of Paediatrics and Child Health workplace based assessment programme. DESIGN:Quality assurance analysis, including gen...

journal_title：Archives of disease in childhood

authors： Archer J,McGraw M,Davies H

更新日期：2010-05-01 00:00:00

abstract：:Cellobiose and mannitol absorption were studied in patients with suspected abnormal function of the small bowel mucosa. The urinary cellobiose:mannitol ratio was increased in subtotal villous atrophy, iron deficiency anaemia, and small intestinal Crohn's disease. The test seems a sensitive indicator of the integrity o...

journal_title：Archives of disease in childhood

authors： Hodges S,Ashmore SP,Patel HR,Tanner MS

更新日期：1989-06-01 00:00:00

abstract：:A 12 year old boy presented with primary nocturnal enuresis. Investigation showed extensive bilateral nephrocalcinosis of no obvious or recognised cause. Persistent severe renal hypercalciuria was confirmed by an intravenous calcium infusion. Idiopathic hypercalciuria is not a common cause of nephrocalcinosis and has ...

journal_title：Archives of disease in childhood

authors： Aggarwal VK,Jones KV

更新日期：1989-07-01 00:00:00

abstract：:After their first episode of febrile convulsions, 195 previously healthy children, aged 6--30 months, were given either diazepam or phenobarbitone for a year. Each child was assigned at random to one of the two medications: children admitted on even days were given a suppository containing 5 mg diazepam every 8 hours ...

journal_title：Archives of disease in childhood

authors： Knudsen FU,Vestermark S

更新日期：1978-08-01 00:00:00

abstract：:Thyroxine (T4) screening values in infants of low birthweight in relation to birthweight and gestational age are reported. There were 86 healthy infants of low birthweight (group 1), and 29 preterm infants with respiratory distress syndrome (group 2). All the group 2 infants and 36% of those in group 1 had a T4 screen...

journal_title：Archives of disease in childhood

authors： Kok JH,Hart G,Endert E,Koppe JG,de Vijlder JJ

更新日期：1983-03-01 00:00:00

abstract：:A child showing signs of Henoch-Schönlein purpura developed a right tibiofibular vascular thrombosis. Antiphospholipid antibody tests were positive for both lupus anticoagulant and anticardiolipin antibodies. This suggests that an antiphospholipid syndrome should be considered in cases of Henoch-Schönlein purpura and ...

journal_title：Archives of disease in childhood

authors： Monastiri K,Selmi H,Tabarki B,Yacoub M,Mahjoub T,Essoussi AS

更新日期：2002-02-01 00:00:00

abstract：:Clinical trials in children in resource-poor environments are essential for local health policy and practice to be relevant and evidence based. Research must be ethical, appropriate, relevant and of good quality. It should, where possible, benefit the subjects studied,the clinical, scientific and support staff involve...

journal_title：Archives of disease in childhood

authors： Molyneux E,Mathanga D,Witte D,Molyneux M

更新日期：2012-09-01 00:00:00

abstract：:A preterm infant with classic phenylketonuria required rather less than 90 mg/kg of phenylalanine and between 270 and 290 mg/kg tyrosine daily to achieve a rate of weight gain of around 20 g/kg per day. Using Lofenalac as the low phenylalanine food, the intake of tyrosine, an essential amino acid for patients with phe...

journal_title：Archives of disease in childhood

authors： Shortland D,Smith I,Francis DE,Ersser R,Wolff OH

更新日期：1985-03-01 00:00:00

abstract：:Interferon is becoming the standard treatment in adults for chronic hepatitis C. Twenty one children with histologically proved chronic hepatitis C (10 boys, range 2.5-13 years), who were otherwise healthy, were enrolled in a randomised controlled study to test their response to interferon alfa. Eleven children were t...

journal_title：Archives of disease in childhood

authors： Iorio R,Pensati P,Porzio S,Fariello I,Guida S,Vegnente A

更新日期：1996-02-01 00:00:00

abstract：:Vision screening of 13 and 15 year old children by school nurses in Oxfordshire has declined in recent years due to the pressure of other commitments. A study was carried out to evaluate the likely consequences of failing to provide vision screening for secondary schoolchildren, in order to make a decision about the f...

journal_title：Archives of disease in childhood

authors： Jewell G,Reeves B,Saffin K,Crofts B

更新日期：1994-01-01 00:00:00

abstract：:Diabetic control in 88 children attending three general paediatric clinics was compared prospectively over one year with that of 89 children attending a specialist paediatric diabetic clinic. Glycated haemoglobin (HbA1) concentration and days admitted were significantly lower in the group attending the specialist clin...

journal_title：Archives of disease in childhood

authors： Bloomfield S,Farquhar JW

更新日期：1990-01-01 00:00:00

abstract：OBJECTIVE:Assays based on interferon gamma (IFNgamma) are an exciting new development for screening for latent tuberculosis infection (LTBI) in adults, but there are limited data on their effectiveness in children. Nevertheless new National Institute for Health and Clinical Excellence (NICE) guidelines recommend their ...

journal_title：Archives of disease in childhood

authors： Taylor RE,Cant AJ,Clark JE

更新日期：2008-03-01 00:00:00

abstract：:The prevalence of wheezing, 'asthma', treatment for 'asthma', and school absence as a result of wheezing in Nottingham was calculated from a questionnaire survey of parents of 4750 children in a random sample of primary schools. A response was achieved for 3805 (80%) children of whom 438 (11.5%) had had episodes of wh...

journal_title：Archives of disease in childhood

authors： Hill RA,Standen PJ,Tattersfield AE

更新日期：1989-02-01 00:00:00

abstract：:Ten intubated neonates (weights 0.90 to 2.58 kg) recovering from respiratory disease had lung mechanics, respiratory patterns, and functional residual capacity measured at 0 cmH2O continuous positive airways pressure and then after application of serially increasing levels of external expiratory resistance. At an exte...

journal_title：Archives of disease in childhood

authors： Moomjian AS,Schwartz JG,Shutack JG,Rooklin AR,Shaffer TH,Fox WW

更新日期：1981-11-01 00:00:00

abstract：:Cytomegalovirus retinitis is common in adults with AIDS but has been reported infrequently in children with perinatally acquired HIV infection. The cases are presented of two infants with vertically acquired HIV infection who developed disseminated cytomegalovirus infection and retinitis, and who posed difficult manag...

journal_title：Archives of disease in childhood

authors： Peters MJ,Moeller HU,Russell-Eggitt I,Novelli V

更新日期：1995-01-01 00:00:00

abstract：:The communication development in 11 children with Angelman's syndrome is described. The clinical observation that these children appear to have a greater ability with receptive rather than expressive language is investigated and these skills assessed using published communication schedules. In addition the understandi...

journal_title：Archives of disease in childhood

authors： Jolleff N,Ryan MM

更新日期：1993-07-01 00:00:00

abstract：AIMS:To examine the disease burden and epidemiology of community acquired rotavirus gastroenteritis in Austrian children treated in a paediatric practice. METHODS:A prospective, population based, multicentre study in four paediatric practices and two children's hospitals (Innsbruck and Leoben). Children

journal_title：Archives of disease in childhood

authors： Frühwirth M,Karmaus W,Moll-Schüler I,Brösl S,Mutz I

更新日期：2001-05-01 00:00:00

abstract：OBJECTIVE:Urolithiasis in renal transplant (RTx) recipients is a potential cause of allograft loss if obstruction is untreated. It is not clear if paediatric transplant recipients are following the global trend for increased prevalence of urolithiasis over time. DESIGN/SETTING/PATIENTS:A retrospective chart review was...

journal_title：Archives of disease in childhood

authors： Ma S,Taher A,Zhu B,Durkan AM

更新日期：2020-01-01 00:00:00

abstract：BACKGROUND:Mauriac syndrome is characterised by growth failure, cushingoid appearance and hepatomegaly which occurs in patients with insulin dependent diabetes and was first described shortly after the introduction of insulin as a treatment for the condition. OBJECTIVE:To describe the clinical features, histological f...

journal_title：Archives of disease in childhood

authors： Fitzpatrick E,Cotoi C,Quaglia A,Sakellariou S,Ford-Adams ME,Hadzic N

更新日期：2014-04-01 00:00:00

abstract：AIM:Ketamine is used for post-operative analgesia. There has been recent disruption in it's supply. It is usually prescribed by patient's weight (3 mg/kg in 50 ml 0.9% saline) at a rate of 1-5 ml/hr (1-5 microgram/kg/minute). To conserve ketamine supplies our policy was changed to a concentrated "standardised" concentr...

journal_title：Archives of disease in childhood

authors： Wong J,Sutherland A

更新日期：2016-09-01 00:00:00

abstract：:The age at which retinopathy of prematurity was first seen was determined in 143 infants. In all, the initial ophthalmological examination was normal. Birth weights varied from 630 to 2700 g and gestational ages from 24.5 to 40.0 weeks. The median postnatal age at which acute retinopathy of prematurity was first seen ...

journal_title：Archives of disease in childhood

authors： Fielder AR,Ng YK,Levene MI

更新日期：1986-08-01 00:00:00

abstract：:In a family in which the father carried a balanced translocation between chromosomes 15 and 22 two of his children had Prader-Willi syndrome and an unbalanced chromosome complement, having lost the proximal bands from the long arm of chromosome 15. His four other surviving children were normal but carried a balanced t...

journal_title：Archives of disease in childhood

authors： Fernandez F,Berry C,Mutton D

更新日期：1987-08-01 00:00:00

abstract：INTRODUCTION:Langerhans cell histiocytosis (LCH) is a rare disease with diverse clinical courses. Despite improvement in survival outcomes in the recent decades, sequelae of the disease remain a concern. This study aimed to provide information on the long-term outcomes in patients with LCH, particularly on the sequelae...

journal_title：Archives of disease in childhood

authors： Chow TW,Leung WK,Cheng FWT,Kumta SM,Chu WCW,Lee V,Shing MMK,Li CK

更新日期：2017-09-01 00:00:00

abstract：:The concentrations of immunoglobulins (Ig) G.A.M. and E were determined in paired umbilical cord and maternal sera in 50 twin pregnancies. Mean IgG levels were higher in cord than maternal sera and in most cases the cord IgG level related more closely to that of the other twin than to either maternal level or birthwei...

journal_title：Archives of disease in childhood

authors： Bryan EM,Slavin B,Nicholson E

更新日期：1976-05-01 00:00:00

abstract：OBJECTIVES:To estimate the incidence of cystic-fibrosis-related diabetes (CFRD) in youth from New South Wales (NSW) and the Australian Capital Territory (ACT), Australia and to examine demographic/clinical features at diagnosis. METHODS:Incident cases of CFRD in young people aged ≤ 18 years diagnosed during 2000 to 20...

journal_title：Archives of disease in childhood

authors： Rana M,Munns CF,Selvadurai HC,Simonds S,Cooper PJ,Woodhead HJ,Hameed S,Verge CF,Lafferty AR,Crock PA,Craig ME

更新日期：2011-09-01 00:00:00

abstract：:Three cases are reported in which thrombi were found in the aorta at postmortem. In each case the thrombus had originated within the ductus arteriosus. We believe that in recent years the attention paid to the presence of indwelling cannulae as a cause of embolic phenomena in the newborn period has led to a reduction ...

journal_title：Archives of disease in childhood

authors： Knowlson GT,Marsden HB

更新日期：1978-02-01 00:00:00

abstract：:A girl was born to a mother who had undergone treatment for epilepsy with carbamazepine during pregnancy. The infant had dysmorphic features and was physically and mentally retarded. We consider that the malformations were the result of the maternal treatment with carbamazepine. ...

journal_title：Archives of disease in childhood

authors： Vestermark V,Vestermark S

更新日期：1991-05-01 00:00:00

abstract：:Three clinically normal sibs were discovered to have type II hyperprolinaemia in a routine serum amino acid screening programme in Sicily. In addition to the basic biochemical features of type II hyperprolinaemia, all 3 children had marked hyperglycinaemia, whereas their parents had both normal blood proline and glyci...

journal_title：Archives of disease in childhood

authors： Pavone L,Mollica F,Levy HL

更新日期：1975-08-01 00:00:00

abstract：:The duration of symptoms before diagnosis (lag time) was defined for 184 of 236 children diagnosed as having a malignancy at the Royal Hospital for Sick Children, Edinburgh for the time period January 1982 until December 1990. The natural logarithm of the lag time was correlated with age, gender, diagnostic group, whi...

journal_title：Archives of disease in childhood

authors： Saha V,Love S,Eden T,Micallef-Eynaud P,MacKinlay G

更新日期：1993-06-01 00:00:00