Published in Helv Paediatr Acta on January 01, 1982
Increasing incidence of coeliac disease in Sweden. Arch Dis Child (1991) 1.01
The changing face of celiac disease. Paediatr Child Health (2001) 0.75
The diagnosis of coeliac disease. A commentary on the current practices of members of the European Society for Paediatric Gastroenterology and Nutrition (ESPGAN). Arch Dis Child (1979) 3.16
[The HIV epidemic: the end of special status]. Rev Med Suisse Romande (1992) 2.45
Childhood celiac disease: a long-term analysis of relapses in 91 patients. J Pediatr Gastroenterol Nutr (1986) 2.14
Ehlers-Danlos syndrome type IV: a multi-exon deletion in one of the two COL3A1 alleles affecting structure, stability, and processing of type III procollagen. J Biol Chem (1988) 1.88
Hepatic capillariasis in a 1-year-old child. Eur J Pediatr (1990) 1.54
Quantitative assessment of exocrine pancreatic function in infants and children. J Pediatr (1968) 1.53
Plasma vitamin C concentrations in patients with cystic fibrosis: evidence of associations with lung inflammation. Am J Clin Nutr (1997) 1.51
Staphylococcal IgE antibodies, hyperimmunoglobulinemia E and Staphylococcus aureus infections. N Engl J Med (1979) 1.47
Immunomodulation by intravenous immunoglobulin. Am J Pediatr Hematol Oncol (1990) 1.46
Epidermolysis bullosa simplex with mottled pigmentation. J Am Acad Dermatol (1989) 1.44
Faecal immunoreactive lipase: a simple diagnostic test for cystic fibrosis. Eur J Pediatr (1998) 1.39
Evaluation of perinatal growth. Presentation of combined intra- and extrauterine growth standards for weight, length and head circumference. Helv Paediatr Acta (1980) 1.35
N-acetylglutamate synthetase deficiency: a disorder of ammonia detoxication. N Engl J Med (1981) 1.31
Familial epilepsy and yellow teeth--a disease of the CNS associated with enamel hypoplasia. Helv Paediatr Acta (1974) 1.26
[Primary hyperparathyroidism in a 12-year-old boy]. Helv Paediatr Acta (1967) 1.21
Kenny syndrome: evidence for idiopathic hypoparathyroidism in two patients and for abnormal parathyroid hormone in one. J Pediatr (1986) 1.19
The syndrome of exocrine pancreatic insufficiency, neutropenia, metaphyseal dysostosis and dwarfism. Helv Paediatr Acta (1969) 1.17
UNICEF/WHO baby-friendly hospital initiative: does the use of bottles and pacifiers in the neonatal nursery prevent successful breastfeeding? Neonatal Study Group. Eur J Pediatr (1997) 1.17
Fecal fat and nitrogen in healthy children and in children with malabsorption or maldigestion. Pediatrics (1970) 1.16
Congenital sensory neuropathy with anhidrosis. Arch Dis Child (1968) 1.12
Spondyloepiphyseal dysplasia, corneal clouding, normal intelligence and acid beta-galactosidase deficiency. Clin Genet (1976) 1.12
Platelet function in congenital afibrinogenemia. Thromb Diath Haemorrh (1965) 1.12
[Automatic blood smear differentiation using the Coulter Electronics Diff 3-50 system]. Schweiz Med Wochenschr (1983) 1.07
PABA screening test for exocrine pancreatic function in infants and children. Arch Dis Child (1978) 1.07
[Diphtheria epidemic in eastern Switzerland in 1974]. Schweiz Med Wochenschr (1977) 1.06
N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxication. Eur J Pediatr (1991) 1.06
Pathogenesis of phenylketonuria: inhibition of DOPA and catecholamine synthesis in patients with phenylketonuria. Clin Chim Acta (1972) 1.04
Transient congenital idiopathic hypoparathyroidism. Helv Paediatr Acta (1967) 1.02
In vivo studies of the phenylalanine-4-hydroxylase system in hyperphenylalaninemics and phenylketonurics. Helv Paediatr Acta (1978) 1.02
Excretion of pterins in phenylketonuria and phenylketonuria variants. Helv Paediatr Acta (1980) 1.02
Catch-up growth in malnutrition, studied in celiac disease after institution of gluten-free diet. Pediatr Res (1972) 1.01
The use of deuterated phenylalanine for the elucidation of the phenylalanine-tyrosine metabolism. Clin Chim Acta (1972) 1.00
The role of calcium in submaxillary saliva of patients with cystic fibrosis. J Pediatr (1967) 0.99
[The course of pregnancy in a representative Swiss population (the Aarau Pregnancy and Newborn Infant Study). I. Social medicine aspects]. Schweiz Med Wochenschr (1985) 0.98
[Hereditary pseudo-vitamin D deficiency rickets]. Helv Paediatr Acta (1969) 0.97
Aagenaes's syndrome in an Italian child. Acta Paediatr Scand (1984) 0.97
[Pregnancy in a representative Swiss population (study of pregnancy and newborn infants in Aarau). 3. Diseases and drugs in pregnancy]. Schweiz Med Wochenschr (1985) 0.96
Neonatal hypocalcaemia. "Early type" in low birth weight newborns. Helv Paediatr Acta (1973) 0.96
[The course of pregnancy in a representative Swiss sample (Aarau Pregnancy and Newborn Infant Study). II. Stimulants in pregnancy]. Schweiz Med Wochenschr (1985) 0.95
Vitamin K1 concentration in breast-fed neonates after oral or intramuscular administration of a single dose of a new mixed-micellar preparation of phylloquinone. J Pediatr Gastroenterol Nutr (1993) 0.95
Systemic lupus erythematosus in Staphylococcus aureus hyperimmunoglobulinaemia E syndrome. Br Med J (Clin Res Ed) (1983) 0.94
Hemolytic-uremic syndrome associated with neuraminidase-producing microorganisms: treatment by exchange transfusion. Helv Paediatr Acta (1980) 0.93
Peptiduria presumably caused by aminopeptidase-P deficiency. A new inborn error of metabolism. J Inherit Metab Dis (1988) 0.93
[Neonatal thrombocyte values in children with Down's syndrome and other autosome trisomies]. Helv Paediatr Acta (1979) 0.93
Iron absorption in cystic fibrosis. Lancet (1965) 0.92
Increased risk of diabetes mellitus in beta- thalassemia major due to iron overload. Helv Paediatr Acta (1979) 0.91
Chronic hypokalaemia with growth retardation, normotensive hyperrenin-hyperaldosteronism ("Bartter's syndrome"), and hypercalciuria. Report of two cases with emphasis on natural history and on catch-up growth during treatment. Helv Paediatr Acta (1971) 0.91
[Weight, length and head circumference of the newborn infant and their relationship to maternal and infant factors. Standards for intrauterine growth]. Helv Paediatr Acta (1980) 0.90
X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22. Hum Genet (1986) 0.90
Survival time in cystinosis. A collaborative study. Proc Eur Dial Transplant Assoc (1983) 0.90
[Blood picture in the early diagnosis of neonatal septicemia]. Helv Paediatr Acta (1976) 0.89
Benign migraine-like syndrome with CSF pleocytosis in children. Dev Med Child Neurol (1985) 0.89
An interstitial deletion of proximal 8q (q11-q13) in a girl with Silver-Russell syndrome-like features. Clin Dysmorphol (1994) 0.89
[The meconium ileus equivalent in mucoviscidosis]. Klin Padiatr (1983) 0.89
Menkes' disease: long-term treatment with copper and D-penicillamine. Eur J Pediatr (1988) 0.88
[Liquid-manure gas intoxication in children using rural latrines]. Schweiz Med Wochenschr (1970) 0.88
Acute mastoiditis: clinical, microbiological, and therapeutic aspects. Eur J Pediatr (1990) 0.88
Hereditary fructose intolerance in early childhood: a major diagnostic challenge. Survey of 20 symptomatic cases. Helv Paediatr Acta (1978) 0.88
Pseudohypoparathyroidism and idiopathic hypoparathyroidism: relationship between serum calcium and parathyroid hormone levels and urinary cyclic adenosine-3',5'-monophosphate response to parathyroid extract. J Clin Endocrinol Metab (1978) 0.87
Congenital lymphoid leukaemia. Case report with chromosomal studies. Helv Paediatr Acta (1968) 0.87
Progressive idiopathic cholestasis presenting with profuse watery diarrhoea and recurrent infections (Byler's disease). Acta Paediatr (1992) 0.86
Enhanced resistance to oxidation of low density lipoproteins and decreased lipid peroxide formation during beta-carotene supplementation in cystic fibrosis. Free Radic Biol Med (1995) 0.86
The immunopathology of coeliac disease. Digestion (1972) 0.86
Infantile lactic acidosis due to hereditary fructose 1,6-diphosphatase deficiency. Helv Paediatr Acta (1971) 0.85
[Quantitative determination of immune globulin maturation by simple radial diffusion method]. Helv Paediatr Acta (1968) 0.85
Long-term low-dose cyclosporin A in steroid dependent nephrotic syndrome of childhood. Eur J Pediatr (1992) 0.84
[Acute celiac disease. Results of studies in 88 patients during 1963 and 1969]. Helv Paediatr Acta (1971) 0.84
Electron microscopic examination of cartilage in the syndrome of exocrine pancreatic insufficiency, neutropenia, metaphyseal dysostosis and dwarfism. Helv Paediatr Acta (1974) 0.83
BCG osteomyelitis. Case report and review. Helv Paediatr Acta (1982) 0.83
Unusual combined immunodeficiency syndrome exhibiting kappa-IgD paraproteinemia, residual gutimmunity and graft-versus-host reaction after plasma infusion. Acta Paediatr Scand (1973) 0.82
[Blood glucose in the full-term newborn infant in the 1st hour following birth]. Helv Paediatr Acta (1982) 0.82
New aspects of infantile oxalosis. Pediatr Nephrol (1987) 0.82
A double-blind comparison of ibuprofen and paracetamol in juvenile pyrexia. Br J Clin Pract Suppl (1990) 0.82
Lactulose: a gas-liquid chromatography method of determination and evaluation of its use to assess intestinal mucosal damage. Clin Chim Acta (1969) 0.82
[Diagnostic significance of lactate concentration in CSF in patients with meningitis (author's transl)]. Dtsch Med Wochenschr (1979) 0.82
[Eye complications in chronic juvenile arthritis]. Klin Monbl Augenheilkd (1993) 0.82
Serum parathyroid hormone concentrations in hypophosphataemic vitamin D resistant rickets. Helv Paediatr Acta (1974) 0.82
Immunological studies of submaxillary saliva from patients with cystic fibrosis and from normal children. J Pediatr (1968) 0.81
Investigations of the kinetics of red cell pyruvate kinase in normal individuals and in a patient with pyruvate kinase deficiency. Nature (1966) 0.81
Long-term results following extensive small intestinal resection in the neonatal period. Prog Pediatr Surg (1977) 0.80
[Metaphyseal dysostosis and congenital pancreatic insufficiency]. Fortschr Geb Rontgenstr Nuklearmed (1968) 0.80
Hypocalcemic fits in neonates. Lancet (1968) 0.80
[Therapy of diabetes insipidus centralis with chlorpropamid (diabinese) and carbamazepin (tegretol) in a child]. Schweiz Med Wochenschr (1972) 0.80
Development of digestive and absorptive function in the human fetus. Nutr Metab (1976) 0.80
[Congenital leukemia with chromosome aberrations (Trisomy G) in a non-mongoloid child]. Helv Paediatr Acta (1974) 0.80
[BCG osteitis in Switzerland. A report of 6 cases]. Schweiz Med Wochenschr (1987) 0.80
[Menkes syndrome]. Ergeb Inn Med Kinderheilkd (1988) 0.80
Neutrophil elastase/alpha 1-proteinase inhibitor complex levels decrease in plasma of cystic fibrosis patients during long-term oral beta-carotene supplementation. Pediatr Res (1996) 0.79
Hydantoin-5-propionic aciduria in folic acid nondependent formiminoglutamic aciduria observed in two siblings. Pediatr Res (1976) 0.79
Letter: 1,25-Dihydroxycholecalciferol in hypoparathyroidism and pseudohypoparathyroidism. Lancet (1975) 0.79
Nature of haemoglobin M-Oldenburg. Nature (1966) 0.79
beta-Mercaptolactate cysteine disulfiduria in two normal sisters. Isolation and characterization of beta-mercaptolactate cysteine disulfide. Clin Chim Acta (1973) 0.79
New mutation in a Swiss girl leading to clinical and biochemical beta-thalassemia minor. Humangenetik (1973) 0.79
Impaired resistance to oxidation of low density lipoprotein in cystic fibrosis: improvement during vitamin E supplementation. Free Radic Biol Med (1995) 0.79
[Transient erythroblastopenia in childhood]. Schweiz Med Wochenschr (1988) 0.79
Variant of hyper-IgE syndrome: the differentiation from atopic dermatitis is important because of treatment and prognosis. Dermatologica (1991) 0.79
Generalized gangliosidosis: acid beta-galactosidase deficiency with early onset, rapid mental deterioration and minimal bone dysplasia. J Neurol (1976) 0.79
Immunthrombocytopenic purpura as a model for pathogenesis and treatment of autoimmunity. Eur J Pediatr (1995) 0.79