Principles of Perinatal–Neonatal Metabolism, 2nd Edition. Edited by Richard M. Cowett (English)
- New search for: Addison, G. M.
- New search for: Addison, G. M.
In:
Journal of Inherited Metabolic Disease
;
22
, 5
;
587
;
1999
- Article (Journal) / Electronic Resource
-
Title:Principles of Perinatal–Neonatal Metabolism, 2nd Edition. Edited by Richard M. Cowett
-
Contributors:Addison, G. M. ( author )
-
Published in:Journal of Inherited Metabolic Disease ; 22, 5 ; 587
-
Publisher:
- New search for: Kluwer Academic Publishers
-
Publication date:1999-06-01
-
Size:1 pages
-
ISSN:
-
DOI:
-
Type of media:Article (Journal)
-
Type of material:Electronic Resource
-
Language:English
-
Source:
Table of contents – Volume 22, Issue 5
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 581
-
Liver transplantation for citrullinaemia improves intellectual functionFletcher, J. M. / Couper, R. / Moore, D. / Coxon, R. / Dorney, S. et al. | 1999
- 587
-
Fasting, postprandial, and post‐methionine‐load homocysteinaemia and methylenetetrahydrofolate reductase polymorphism in vascular diseaseCandito, M. / Bedoucha, P. / Gibelin, P. / Jambou, D. / de Franchis, R. / Sadoul, J.‐L. / Chatel, M. / Van Obberghen, E. et al. | 1999
- 587
-
Principles of Perinatal–Neonatal Metabolism, 2nd Edition. Edited by Richard M. CowettAddison, G. M. et al. | 1999
- 592
-
Manual of Metabolic Diseases. Mohammed A. Al‐Elessa and Pinar T. OzandCleary, M. A. et al. | 1999
- 593
-
3‐Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh diseaseDi Rocco, M. / Caruso, U. / Moroni, I. / Lupino, S. / Lamantea, E. / Fantasia, A. R. / Borrone, C. / Gibson, K. M. et al. | 1999
- 598
-
An Atlas of Common Metabolic and Genetic Diseases. Mohammed A. Al‐Elessa, Nadia A. Sakati, Pinar T. OzandCleary, M. A. et al. | 1999
- 599
-
Progressive neurological deterioration and MRI changes in cblC methylmalonic acidaemia treated with hydroxocobalaminEnns, G. M. / Barkovich, A. J. / Rosenblatt, D. S. / Fredrick, D. R. / Weisiger, K. / Ohnstad, C. / Packman, S. et al. | 1999
- 608
-
Single‐cell analysis of mitochondrial DNA in patients and a carrier of the tRNALeu(UUR) gene mutationSaitoh, S. / Momoi, M. Y. / Yamagata, T. / Nakauchi, H. / Nihei, K. / Fujii, M. et al. | 1999
- 615
-
Personality profiles of mothers of children with mitochondrial disordersVarvogli, L. / Waisbren, S. E. et al. | 1999
- 623
-
Intracellular degradation of fluorescent glycolipids by lysosomal enzymes and their activatorsMadar‐Shapiro, L. / Pasmanik‐Chor, M. / Dinur, T. / Dagan, A. / Gatt, S. / Horowitz, M. et al. | 1999
- 638
-
Long‐term follow‐up following bone marrow transplantation for Hunter diseaseVellodi, A. / Young, E. / Cooper, A. / Lidchi, V. / Winchester, B. / Wraith, J. E. et al. | 1999
- 649
-
Ceramide accumulation is associated with increased apoptotic cell death in cultured fibroblasts of sphingolipid activator protein‐deficient mouse but not in fibroblasts of patients with Farber diseaseTohyama, J. / Oya, Y. / Ezoe, T. / Vanier, M. T. / Nakayasu, H. / Fujita, N. / Suzuki, K. et al. | 1999
- 663
-
Recurrent rhabdomyolysis in a child with glutaric aciduria type IWilson, C. J. / Collins, J. E. / Leonard, J. V. et al. | 1999
- 663
-
Recurrent rhabdomyolysis in a child with glutaric aciduria type 1Wilson, C. J. / Collins, J. E. / Leonard, J. V. et al. | 1999
- 665
-
NTBC as palliative treatment in chronic tyrosinaemia type IRos, J. / Vilaseca, M. A. / Lambruschini>, N. / Mas, A. / Lindstedt, S. / Holme, E. et al. | 1999
- 665
-
NTCB as palliative treatment in chronic tyrosinaemia type IRos, J. / Vilaseca, M. A. / Lambruschini, N. / Alas, A. / Lindstedt, S. / Holme, E. et al. | 1999
- 666
-
Early‐infantile type of galactosialidosis as a cause of heart failure and neonatal ascitesClaeys, M. / Van Der Hoeven, M. / de Die‐Smulders>, C. / Bakker, J. A. / Offermans, J. P. M. / Forget, P‐Ph. / Groener, J. E. M. / Spaapen, L. J. M. et al. | 1999
- 668
-
A case with early infantile form of galactosialidosis with unusual haematological findingsTekinalp, G. / Aliefendioğlu, D. / Yüce, A. / çağlar, M. / Beck, M. et al. | 1999
- 670
-
Absence of apolipoprotein B3500 mutation in type 2a hyperlipoproteinemia patients and in the general population from Southern ItalySeripa, D. / Gravina, C. / Volpe, R. / Margaglione, M. / Papa, S. / Merla, G. / Parrella, P. / Di Minno, G. / Ricci, G. / Testa, M. et al. | 1999
- 670
-
Absence of apolipoprotein B3500 mutation in type 2a hyperlipoproteinaemia patients and in the general population from Southern ItalySeripa, D. / Gravina, C. / Volpe, R. / Margaglione, M. / Papa, S. / Merla, G. / Parrella, P. / Di Minno, G. / Ricci, G. / Testa, M. et al. | 1999
- 672
-
Ornithine carbamoyltransferase deficiency: Unusual clinical findings and novel mutationShih, V. E. / Safran, A. P. / Ropper, A. H. / Tuchman, M. et al. | 1999
- 674
-
Is the common 844ins68 polymorphism in the cystathionine β‐synthase gene associated with atherosclerosis?Orendáč, M. / Mušková, B. / Richterová, E. / Zvárová, J. / Štefek, M. / Zaykova, E. / Kraus, J. P. / Stříbrný, J. / Hyánek, J. / Kožich, V. et al. | 1999
- 676
-
A 84 bp insertion found in a propionic acidaemia patient is not a disease-causing mutation but a product of cryptic mRNAOhura, T. / Narisawa, K. / Tada, K. / Iinuma, K. et al. | 1999
- 676
-
An 84bp insertion found in a propionic acidaemia patient is not a disease‐causing mutation but a product of cryptic mRNAOhura, T. / Narisawa, K. / Tada, K. / Iinuma, K. et al. | 1999
- 677
-
Enantiomeric analysis of D‐ and L‐pipecolic acid in plasma using a chiral capillary gas chromatography column and mass fragmentographyStruys, E. A. / Jakobs, C. et al. | 1999
- 679
-
Molecular characterization of Polish patients with classical galactosaemia IZekanowski, C. / Radomyska, B. / Bal, J. et al. | 1999
- 679
-
Molecular characterization of Polish patients with classical galactosaemiaŻdekanowski, C. / Radomyska, B. / Bal, J. et al. | 1999
- 682
-
A novel exonic mutation in the aspartylglucosaminidase gene causes exon skippingCoulter‐Mackie, M. B. et al. | 1999