Clinical Quiz
Joseph F. Fitzgerald
NASPGHAN Clinical Quiz Editor
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorRiccardo Troncone
ESPGHAN Clinical Quiz Editor
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorPaola Roggero
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorElena Pozzi
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorBarbara Garavaglia
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorRossella Parini
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorEmanuela Carissimi
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorFrancesca Santus
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorPasqua Piemontese
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorElena Cataliotti
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorFabio Mosca
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorVittorio Carnelli
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorContributors
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorJoseph F. Fitzgerald
NASPGHAN Clinical Quiz Editor
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorRiccardo Troncone
ESPGHAN Clinical Quiz Editor
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorPaola Roggero
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorElena Pozzi
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorBarbara Garavaglia
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorRossella Parini
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorEmanuela Carissimi
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorFrancesca Santus
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorPasqua Piemontese
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorElena Cataliotti
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorFabio Mosca
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorVittorio Carnelli
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this authorContributors
Paediatrics Department University Medical School Milan, Italy, Division of Biochemestry and Genetics, National Institute of Neurology “Carlo Besta”, Milan, Italy
Search for more papers by this author
REFERENCES
- 1Lerner A, Gruener N, Iancu TC. Serum carnitine concentrations in coeliac disease. Gut 1993; 34: 933–35.
- 2Duran M, Loof NE, Ketting D, et al. Secondary carnitine deficiency. J Clin Chem & Clin Biochem 1990; 28: 359–63.
- 3Pons R, De Vivo DC. Primary and secondary carnitine deficiency syndromes. J Child Neurol 1995; 10 Suppl 2: S8–24.
- 4Garavaglia B, Uziel G, Dworzak F, et al. Primary carnitine deficiency: heterozygote and intrafamilial phenotypic variation. Neurology 1991; 41: 1691–93.
- 5Wos H, Grzybowska-Chlebowczyk U, Bujniewicz E. Plasma carnitine concentration in children with classic coeliac disease. J Pediatr Gastroenterol Nutr 2001; 32: 379.
- 6Roggero P, Pozzi E, Cataliotti E, et al. Coeliac disease as a cause of secondary carnitine deficiency. J Pediatr Gastroenterol Nutr 2001; 32: 370.
- 7Bonamico M, Pitzalis G, Ballati G, et al. Il comportamento della carnitina sierica in bambini affetti da malattia celiaca. Riv Ital Pediatr 1987; 13: 104.
