听力与言语-语言病理学

行为科学

医学伦理学

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  • Complement studies in children with treated coeliac disease after gluten challenge.

    abstract::Changes of the complement components in the sera of 13 children with treated coeliac disease were studied after gluten challenge. The levels of C 1 and C3-activator (factor B) were significantly decreased at 4 h after the challenge, as were the levels of total complement (CH 50) and the components C 1, C 4 and C 1-ina...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF01846034

    authors: Bosch C,Becker M,Rotthauwe HW,Opferkuch W

    更新日期:1980-08-01 00:00:00

  • Hypoketosis as a cause of symptoms in childhood hypoglycemia.

    abstract::Children with symptomatic hypoglycemia and asymptomatic hypoglycemia-prone children were shown to differ in the degree of ketosis after a 20 h fast. In the latter children the close negative correlation between ketone body levels and glucose levels yielded a regression line against which the former children's data cou...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00442403

    authors: Teijema HL,van Gelderen HH,Giesberts MA

    更新日期:1980-06-01 00:00:00

  • Achondrogenesis type I: light and electron-microscopic studies.

    abstract::The light- and electron-microscopic structure of articular and costal cartilage in a case of achondrogenesis type I has been described. The most characteristic ultrastructural change in the chondrocytes was conspicuous dilatation of the rough endoplasmatic reticulum (RER) which contained amorphous electronopaque mater...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00442406

    authors: Molz G,Spycher MA

    更新日期:1980-06-01 00:00:00

  • Urinary oligosaccharide screening in patients with beta-galactosidase deficiency.

    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

    pub_type: 杂志文章

    doi:10.1007/BF00496087

    authors: Sewell AC,Gehler J,Spranger J

    更新日期:1980-05-01 00:00:00

  • Poly-, syn- and oligodactylyl, aplasia or hypoplasia of fibula, hypoplasia of pelvis and bowing of femora in three sibs--a new autosomal recessive syndrome.

    abstract::An apparently hitherto undescribed, severe skeletal syndrome is reported in 3 siblings (2 boys, 1 girl) in a family of Turkish-Arabian descent. Major manifestations include: hypoplasia of the pelvis, congenital dislocation of the hip, severe bowing of femora, aplasia or hypoplasia of fibulae, absence or coalescence of...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441580

    authors: Fuhrmann W,Fuhrmann-Rieger A,de Sousa F

    更新日期:1980-03-01 00:00:00

  • Quantitative measurements of the urinary excretion of creatinine, uric acid, hypoxanthine and xanthine, uracil, cyclic AMP, and cyclic GMP in healthy newborn infants.

    abstract::Serum creatinine, uric acid, and hypoxanthine and xanthine concentrations were determined in 17 mother-infant pairs at the time of delivery. Creatinine and uric acid levels were nearly similar, but hypoxanthine and xanthine were more than twice as high in the blood of the infants than in the blood of their mothers. In...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441585

    authors: Manzke H,Spreter von Kreudenstein P,Dörner K,Kruse K

    更新日期:1980-03-01 00:00:00

  • Everything the pediatrician ever wanted to know about HLA but was afraid to ask.

    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

    pub_type: 杂志文章,评审

    doi:10.1007/BF00441576

    authors: Passarge E,Valentine-Thon E

    更新日期:1980-03-01 00:00:00

  • Chromosome deletion and multiple cartilaginous exostoses.

    abstract::We report a 13 year-old girl with manifestations strikingly reminiscent of the tricho-rhino-phalangeal (TRP) II or Langer-Giedion syndrome. A terminal deletion of 8q must be assumed to be the cause of her condition till proven otherwise. A similar chromosome abnormality should be searched for (blindly) in other cases ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441586

    authors: Bühler EM,Bühler UK,Stalder GR,Jani L,Jurik LP

    更新日期:1980-03-01 00:00:00

  • Efficiency of heparin in the treatment of newborn infants with respiratory distress syndrome and disseminated intravascular coagulation.

    abstract::Forty newborns with severe shock and disseminated intravascular coagulation were randomized for treatment with heparin or placebo. Mortality was equal in both groups. The heparin group required significantly shorter periods of artificial ventilation. The coagulation system improved faster, and the coagulation pattern ...

    journal_title:European journal of pediatrics

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1007/BF00444754

    authors: Göbel U,von Voss H,Jürgens H,Petrich C,Pothmann R,Sprock I,Lemburg P

    更新日期:1980-01-01 00:00:00

  • Evaluation of the indications for early exchange transfusion in rhesus haemolytic disease during phototherapy.

    abstract::The study material consisted of 251 newborn light-treated infants with rhesus haemolytic disease (RHD) caused by anti-D. 139 infants were treated with ordinary phototherapy (white single light) and 112 infants with intensive phototherapy (blue double light). An evaluation was made as to wheter the indications for earl...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00444752

    authors: Ebbesen F

    更新日期:1980-01-01 00:00:00

  • Investigation of accelerated metabolic function in small for gestational age infants.

    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

    pub_type: 杂志文章

    doi:10.1007/BF00442433

    authors: von Stockhausen HB,Struve M

    更新日期:1979-11-01 00:00:00

  • Unusual roentgenographic presentation of a congenital cystic malformation of the lung.

    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

    pub_type: 杂志文章

    doi:10.1007/BF00447379

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

    更新日期:1979-10-01 00:00:00

  • Diaphragmatic hernia in a female newborn with focal dermal hypoplasia and marked asymmetric malformations (Goltz-Gorlin syndrome).

    abstract::We report a female newborn with focal dermal hypoplasia (Goltz-Gorlin Syndrome) and marked asymmetric malformations on the right side of the body. Diaphragmatic hernia on the same side, which has not been reported in this syndrome, led to perinatal complications. ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00538945

    authors: Kunze J,Heyne K,Wiedemann HR

    更新日期:1979-06-28 00:00:00

  • Benign cystic nephroblastoma.

    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

    pub_type: 杂志文章

    doi:10.1007/BF00447474

    authors: Havers W,Stambolis C

    更新日期:1979-05-18 00:00:00

  • Evaluation of long term tobramycin therapy in patients with cystic fibrosis and advanced pulmonary disease.

    abstract::To nine cystic fibrosis patients with chronic bronchopulmonary infection of severely damaged lungs invaded by Pseudomonas aeruginosa, eleven courses of prolonged tobramycin treatment (5 mg/kg/day) for four to 16 weeks were administered. Pulmonary symptoms improved and a better quality of life was achieved in all but o...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441362

    authors: Paporisz U,Posselt HG,Wönne R,Ristow W,Röser D,Knothe H,Bender SW

    更新日期:1979-04-03 00:00:00

  • A new method for screening for hyperammonemia.

    abstract::A new method for the detection of hyperammonemia, using a kit based on the principle of microdiffusion of ammonia, is described. The method requires only one drop of blood and takes only 15 min to complete. Experiments for recovery and reproducibility were satisfactory, and good correlation was obtained when compared ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00442347

    authors: Tada K,Okuda K,Watanabe K,Iimura Y,Yamada S

    更新日期:1979-02-08 00:00:00

  • Rheumatoid arthritis and growth retardation in children: treatment with human growth hormone.

    abstract::Twenty patients with rheumatoid arthritis or Still's disease associated with growth failure were treated with human growth hormone, 7.5 to 17 U/m2 body surface per week. Five patients did not respond with better growth. In the remainder the mean growth rate increased from 1.9 cm/year (range: 0 to 3.3) to 6.2 cm/year (...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441894

    authors: Butenandt O

    更新日期:1979-01-18 00:00:00

  • Development of children with early cytomegalovirus infection.

    abstract::To find out whether cytomegalovirus (CMV) infection during the first months of life influences child development, developmental assessment at the age of 2 years was performed on 116 Finnish children chosen at random in a maternity hospital and followed from birth for the occurrence of CMV infection. Two of the childre...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00496851

    authors: Granström ML

    更新日期:1979-01-01 00:00:00

  • Design of a multiple longitudinal study of growth and health in teenagers.

    abstract::This paper describes the design of a study to follow the development of boys and girls in secondary schools from the age of 12 through 17 on an annual basis, in order to acquire more information concerning the growth and development of teenagers. In this study, both physical and psychological characteristics are measu...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00442158

    authors: Kemper HC,van 't Hof MA

    更新日期:1978-10-12 00:00:00

  • Hyperphenylalaninaemia due to dihydropteridine reductase deficiency.

    abstract::Two siblings with increased levels of serum phenylalanine were detected by newborn screening. The older sibling deteriorated neurologically and mentally, despite early dietary control, and died at the age of 6 1/2 years. In the younger sibling phenylalanine hydroxylase activity in liver tissue was normal. Further inve...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00442368

    authors: Gröbe H,Bartholome K,Milstien S,Kaufman S

    更新日期:1978-09-08 00:00:00

  • Anatomy of the naso-lacrimal duct in new-borns: therapeutic considerations.

    abstract::The topography and morphology of the lacrimal ducts in newborn infants was demonstrated by means of post mortem dacryocystograms and microphotograms of histologic slides. Because of bends in the course of the lower tear duct, a percentage of probings will fail to effect satisfactory perforation of the Hasner membrane....

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00442367

    authors: Müller KM,Busse H,Osmers F

    更新日期:1978-09-08 00:00:00

  • Mucopolysaccharidosis II (Hunter disease) with corneal opacities. Report on two patients at the extremes of a wide clinical spectrum.

    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

    pub_type: 杂志文章

    doi:10.1007/BF00441369

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

    更新日期:1978-08-17 00:00:00

  • Argininosuccinic aciduria: metabolic studies and effects of treatment with keto-analogues of essential amino acids.

    abstract::A 22 years old female with the late-onset of argininosuccinic aciduria was successfully treated for 5 months with a mixture of essential amino acids and their keto-analogues. There was a marked change in plasma ammonia, plasma amino acids and argininosuccinic acid excretion. A long term anabolic response was reflected...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00445607

    authors: Böhles H,Heid H,Harms D,Schmid D,Fekl W

    更新日期:1978-07-19 00:00:00

  • Factor VIII activity and factor VIII related antigen in newborns.

    abstract::Factor VIII procoagulant activity and factor VIII related antigen were examined in 20 full-term and preterm newborn infants during the first days of life. The control group involved 15 adults volunteers. Factor VIII activity was estimated by a one-stage test and factor VIII related antigen was determined by immunelect...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00445613

    authors: Maak B,Scheidt B,Frenzel J

    更新日期:1978-07-19 00:00:00

  • Glucocorticosteroids and growth hormone secretion under physiological conditions and in states of steroid excess.

    abstract::Cortisol and growth hormone (GH) secretion (spontaneous variations at night and the release induced by insulin hypoglycaemia) were investigated in 69 children and adolescents. Statistical analysis of approximately 600 pairs of cortisol and GH values in this study demonstrated that physiological fluctuations of cortiso...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00496996

    authors: Mühlendahl KE,Weber B,Müller-Hess R,Korth-Schütz S,Helge H

    更新日期:1978-06-20 00:00:00

  • Vascular origin of Poland syndrome? A comparative rheographic study of the vascularisation of the arms in eight patients.

    abstract::Vascularization of the arms has been studied by impedance plethysmography (rheography) in eight children with Poland syndrome, a common malformation characterized by unilateral hand anomaly and ipsilateral aplasia of the inferior head of the pectoralis major muscle. A marked decrease of the velocity of the systolic in...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00496922

    authors: Bouvet JP,Leveque D,Bernetieres F,Gros JJ

    更新日期:1978-05-22 00:00:00

  • The Zellweger syndrome: subcellular pathology, neuropathology, and the demonstration of pneumocystis carinii pneumonitis in two siblings.

    abstract::The first Scandinavian cases of Zellweger syndrome (ZS) are described. A brother and sister, children of first cousins, had the typical clinical symptoms and pathological findings. Extensive metabolic studies in the boy were negative. Pipecolic acid in the urine was not elevated. Both children died at 14 weeks of age....

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00493539

    authors: Brun A,Gilboa M,Meeuwisse GW,Nordgren H

    更新日期:1978-04-20 00:00:00

  • Serum lysozyme activity in children with acute leukemia.

    abstract::Serum lysozyme activity was measured in samples from children with acute leukemia, malignant tumours, and in normal children. All children with acute lymphatic leukemia (ALL) had significantly reduced levels of lysozyme at diagnosis, and none of the children fell within the normal range. Children with ALL in complete ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00493542

    authors: Bratlid D,Moe PJ

    更新日期:1978-04-20 00:00:00

  • Treatment of seven cases of chronic granulomatous disease with sulfamethoxazole-trimethoprim (SMX-TMP).

    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

    pub_type: 杂志文章

    doi:10.1007/BF00493540

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

    更新日期:1978-04-20 00:00:00

  • Hyaline membrane disease: prognostic factors and medium-term follow-up.

    abstract::One hundred and twenty two cases of severe hyaline membrane disease are reported. 68 of them survived (57%). Adverse clinical, radiological and laboratory factors, and their effects on the early mortality rate, are analysed with particular reference to the referring centers, delay in admission, transport and the criti...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00442059

    authors: Goenen M,Ninane J,Ducoffre B,Declerck Y,Claus D,Ferriere G,Thomas-van Moerbeke RM,Moulin D,De Meyer R,Tremouroux J

    更新日期:1978-03-13 00:00:00

  • Haemorrhagic diathesis as a possible early sign of hereditary fructose intolerance.

    abstract::An infant girl three weeks of age with the leading symptom of skin haemorrhages is presented. On further investigation, the signs of severe hepatic damage with hypofibrinogenaemia and prothrombin complex impairment, and renal tubular dysfunction were disclosed. All these pathological symptoms, which were reversed on f...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00465567

    authors: Hosková A,Mrskos A

    更新日期:1977-12-30 00:00:00

  • Therapeutic and collateral effects of 25-hydroxycholecalciferol in vitamin D deficiency.

    abstract::The clinical and biochemical response to 25-hydroxycholecalciferol (25-HCC) and vitamin D3, 150 microgram/day for 20 days has been compared in infants aged 3--18 months with nutritional rickets. The infants were allocated at random to Group I (11 infants) treated with 25HCC and Group II (9 infants) treated with vitami...

    journal_title:European journal of pediatrics

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1007/BF00465565

    authors: Moya M,Beltran J,Colomer J

    更新日期:1977-12-30 00:00:00

  • Generalized oedema of newborn associated with the administration of dipyrone.

    abstract::In fourteen infants, aged 9--60 days, with generalized oedema seen during a one year period the common denominator was the administration of dipyrone one to two days prior to the development of oedema. None of the other causes of oedema in early life could be incriminated in any of these babies. Pediatricians should b...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00477053

    authors: Bajoghli M,Ajudani TS,Gharavi M

    更新日期:1977-11-04 00:00:00

  • Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findings.

    abstract::The pre- and postnatal clinical, cytogenetic and embryological findings in a family suffering from trisomy 9p and spinal muscular atrophy are presented. The clinical picture of the "trisomy 9p" -syndrome is delineated. Concurrence of autosomal aberration and spinal muscular atrophy, probably of the Werdnig-Hoffmann ty...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00443119

    authors: Tolksdorf M,Kunze J,Gross-Selbeck G,Sperling K,Wegner RD,Wieczorek V,Vogel M

    更新日期:1977-08-23 00:00:00

  • The influence of perinatal risk factors on the incidence of atypical coagulation factor VII during the first days of life.

    abstract::The correlation between the appearance of functionally-atypical factor VII and perinatal complications was investigated in 66 newborn infants. The presence of an abnormal clotting factor was assumed if the ratio between clotting activity and antigen-related factor VII material exceeded the normal range for adult plasm...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00493570

    authors: Maak B,Frenzel J

    更新日期:1977-08-12 00:00:00

  • Accuracy of blood volume estimations in critically ill children using 125I-labelled albumin and 51Cr-labelled red cells.

    abstract::Blood volume was estimated using 51chromium labelled red cells and 125iodinated human serum albumin in 5 children with sepsis, in 6 burned children and 7 children with acute lymphoblastic leukaemia. Studies of the equilibration pattern demonstrated that the mixing time of labelled red cells was prolonged to 40 minutes...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00489987

    authors: Linderkamp O,Holthausen H,Seifert J,Butenandt I,Riegel KP

    更新日期:1977-06-01 00:00:00

  • A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantile cirrhosis with hemosiderosis.

    abstract::A patient with a cerebro-hepato-renal syndrome was investigated. The visceral manifestations were those of the Zellweger syndrome (ZS); however, the child exhibited muscular hypertonia and survived into the 2nd year of life. Ultramicroscopically, hepatocytes were lacking peroxisomes, but, contrary to findings in one p...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441934

    authors: Versmold HT,Bremer HJ,Herzog V,Siegel G,Bassewitz DB,Irle U,Voss H,Lombeck I,Brauser B

    更新日期:1977-03-18 00:00:00

  • On the influence of age on immunity in Down's syndrome.

    abstract::In 23 subjects of different ages with Down's syndrome a number of parameters of non-specific defense of humoral and cellular immunity were investigated. While in all age groups complement factors C3, C4 and C5 as well as phagocytosis and NBT indices were in the normal range, a dysgammaglobulinaemia increasing with age...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00477543

    authors: Seger R,Buchinger G,Ströder J

    更新日期:1977-01-26 00:00:00

  • Bone marrow hypoplasia in anorexia nervosa.

    abstract::Within a 2-year period, from March 1974 until May 1976 10 patients with anorexia nervosa were seen at the children's university hospitals of München (2 patients) and Giessen (8 patients). The patients were 10-16 years old, with one exception all girls, and had the typical cachexia, hypothermia, bradycardia, gray, hair...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00452416

    authors: Lampert F,Lau B

    更新日期:1976-12-09 00:00:00

  • Studies of malformation syndromes of man XXXXIIB: mother and son affected with the ulnar-mammary syndrome type Pallister.

    abstract::We report mother and son with the ulnar-mammary syndrome type Pallister: both had postaxial polydactyly in one upper limb and absence or hypoplasia of the axillary apocrine glands bilaterally. The mother had total lack of the mammary gland tissue and absence of one kidney. Her son also had unilateral oligodactyly, an ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00444644

    authors: Gonzalez CH,Herrmann J,Opitz JM

    更新日期:1976-11-03 00:00:00

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