Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria.

I Smith, M. E. Lobascher, Jamie Stevenson, +4

BMJ

NutritionBody CompositionIntellectual ProgressNutritional RequirementInherited Metabolic Disease +12

Neurological outcome in adult patients with early-treated phenylketonuria

J. Pietz, Robert Dunckelmann, André Rupp, +4

European Journal of Pediatrics

Neurological DisorderClinical NeurologyNeurological OutcomeNeurologyNeuropathology +2

Atypical phenylketonuria due to tetrahydrobiopterin deficiency. Diagnosis and treatment with tetrahydrobiopterin, dihydrobiopterin and sepiapterin

H.‐Ch. Curtius, A. Niederwieser, M. Viscontini, +4

Clinica Chimica Acta

Atypical PhenylketonuriaUrologyMedicineInherited Metabolic DiseaseChronic Kidney Disease

The diagnostic value of urinary pyridinium cross-links of collagen, serum total alkaline phosphatase, and urinary calcium excretion in neoplastic bone disease.

Martin Pecherstorfer, Ilse Zimmer-Roth, Tobias Schilling, +6

The Journal of Clinical Endocrinology & Metabolism

Affect Skeletal MetabolismPathologyOsteoporosisBone DiseaseCancer Metabolism +15

Development of height and weight in children with diabetes mellitus: Report on two prospective multicentre studies, one cross-sectional, one longitudinal

A. Thon, E. Heinze, K. Feilen, +5

European Journal of Pediatrics

ObesityMetabolic SyndromeChildhood ObesityDiabetes EpidemiologyProspective Multicentre Studies +7

Serotonin and Dopamine Synthesis in Phenylketonuria

H.‐Ch. Curtius, A. Niederwieser, M. Viscontini, +6

Advances in experimental medicine and biology

Dopamine SynthesisMedicineNeurotransmitterNeuroscienceNervous System +2

Growth and skeletal maturation in children with phenylketonuria

Franz Schaefer, Peter Burgard, U. Batzler, +5

Acta Paediatrica

Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuria

Peter Burgard, André Rupp, David Konecki, +3

European Journal of Pediatrics

Residual Enzyme ActivityUrologyBiochemistryPhenotypic ParametersMedicine +3

Prenatal diagnosis of ?dihydrobiopterin synthetase? deficiency, a variant form of phenylketonuria

A. Niederwieser, Haruo Shintaku, Th. Hasler, +4

European Journal of Pediatrics

UrologyGenetic DisorderInherited Metabolic DiseasePediatricsVariant Form +3

Skeletal findings in homocystinuria: A collaborative study

H Schedewie, E. Willich, H. Gr�be, +2

Pediatric Radiology

Axial SkeletonHistopathologySkeletal FindingsPathologyAnatomy +3