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Volume 163, Number 10, October 2004

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Clinical and biochemical manifestations of syndrome X in obese children
pp. 573-579(7)
Authors: Papadopoulou-Alataki, Efimia; Papadopoulou-Legbelou, Kiriaki; Doukas, Loukas; Karatzidou, Kiparissia; Pavlitou-Tsiontsi, Aikaterini; Pagkalos, Emmanouil

Hypothalamic adipic hypernatraemia syndrome with normal osmoregulation of vasopressin
pp. 580-583(4)
Authors: López-Capapé, Marta; Golmayo, Luz; Lorenzo, Gustavo; Gallego, Nieves; Barrio, Raquel

Irritable bowel syndrome: the commonest cause of recurrent abdominal pain in children
pp. 584-588(5)
Authors: El-Matary, Wael; Spray, Christine; Sandhu, Bhupinder

Neonatal severe hyperparathyroidism: genotype/phenotype correlation and the use of pamidronate as rescue therapy
pp. 589-594(6)
Authors: Waller, Simon; Kurzawinski, Tom; Spitz, Lewis; Thakker, Rajesh; Cranston, Treena; Pearce, Simon; Cheetham, Tim; Hoff, William

Monitoring the clinical and biochemical response to enzyme replacement therapy in three children with Fabry disease
pp. 595-603(9)
Authors: Mills, Kevin; Vellodi, Ashok; Morris, Peter; Cooper, Donald; Morris, Michael; Young, Elisabeth; Winchester, Bryan

Chronic mucocutaneous candidiasis and primary hypothyroidism in two families
pp. 604-611(8)
Authors: Myhre, Anne; Stray-Pedersen, Asbjørg; Spangen, Steinar; Eide, Eigill; Veimo, Dag; Knappskog, Per; Abrahamsen, Tore; Husebye, Eystein

Inherited multicentric osteolysis with carpal-tarsal localisation mimicking juvenile idiopathic arthritis
pp. 612-618(7)
Authors: Faber, Marianne; Verlaak, René; Fiselier, Theo; Hamel, Ben; Franssen, Marcel; Gerrits, G.

Percutanous closure of patent ductus arteriosus in small infants of less than 8 kg body weight using different devices
pp. 619-621(3)
Authors: Knirsch, Walter; Haas, Nikolaus; Lewin, Martin; Dähnert, Ingo; Kececioglu, Deniz; Berger, Felix; Uhlemann, Frank

Hearing impairment in familial X-linked hypophosphatemic rickets
pp. 622-623(2)
Authors: Fishman, Gadi; Miller-Hansen, Denise; Jacobsen, Cynthia; Singhal, Virender; Alon, Uri

Prognostic factors for mortality of oesophageal atresia patients: Waterston revived
pp. 624-625(2)
Authors: Deurloo, Jacqueline; Vos, Rien; Ekkelkamp, Seine; Heij, Hugo; Aronson, Daniel

Leukaemia presenting with fulminant hepatic failure in a child
pp. 628-629(2)
Authors: Kader, Ajmal; Vara, Roshni; Egberongbe, Yaya; Height, Sue; Dhawan, Anil

The infrequent bowel movements in young infants who are exclusively breast-fed
pp. 630-631(2)
Authors: Choe, Yon; Lee, Ji; Moon, Kwang; Hwang, Jong; Seo, Jeong

Diagnostic evaluation for asymmetry: consider genetic mosaicism
pp. 634-635(2)
Authors: Devriendt, Koen; Fryns, Jean-Pierre

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