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Journal Abstract Search
159 related items for PubMed ID: 9309516
1. Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a second family. Maller A, Hyland K, Milstien S, Biaggioni I, Butler IJ. J Child Neurol; 1997 Sep; 12(6):349-54. PubMed ID: 9309516 [Abstract] [Full Text] [Related]
2. Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a new inborn error of neurotransmitter amine synthesis. Hyland K, Surtees RA, Rodeck C, Clayton PT. Neurology; 1992 Oct; 42(10):1980-8. PubMed ID: 1357595 [Abstract] [Full Text] [Related]
6. Abnormalities of biogenic amines affecting the metabolism of serotonin and catecholamines. Lamers KJ, Wevers RA. Mult Scler; 1998 Feb; 4(1):37-8. PubMed ID: 9532591 [Abstract] [Full Text] [Related]
7. A rare cause of severe diarrhoea diagnosed by urine metabolic screening: aromatic L-amino acid decarboxylase deficiency. Lee LK, Cheung KM, Cheng WW, Ko CH, Lee HH, Ching CK, Mak C. Hong Kong Med J; 2014 Apr; 20(2):161-4. PubMed ID: 24714172 [Abstract] [Full Text] [Related]
9. Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. Pons R, Ford B, Chiriboga CA, Clayton PT, Hinton V, Hyland K, Sharma R, De Vivo DC. Neurology; 2004 Apr 13; 62(7):1058-65. PubMed ID: 15079002 [Abstract] [Full Text] [Related]
10. Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency. Brun L, Ngu LH, Keng WT, Ch'ng GS, Choy YS, Hwu WL, Lee WT, Willemsen MA, Verbeek MM, Wassenberg T, Régal L, Orcesi S, Tonduti D, Accorsi P, Testard H, Abdenur JE, Tay S, Allen GF, Heales S, Kern I, Kato M, Burlina A, Manegold C, Hoffmann GF, Blau N. Neurology; 2010 Jul 06; 75(1):64-71. PubMed ID: 20505134 [Abstract] [Full Text] [Related]
11. Aromatic l-aminoacid decarboxylase deficiency: unusual neonatal presentation and additional findings in organic acid analysis. Abdenur JE, Abeling N, Specola N, Jorge L, Schenone AB, van Cruchten AC, Chamoles NA. Mol Genet Metab; 2006 Jan 06; 87(1):48-53. PubMed ID: 16288991 [Abstract] [Full Text] [Related]
12. Aromatic L-amino acid decarboxylase deficiency with hyperdopaminuria. Clinical and laboratory findings in response to different therapies. Fiumara A, Bräutigam C, Hyland K, Sharma R, Lagae L, Stoltenborg B, Hoffmann GF, Jaeken J, Wevers RA. Neuropediatrics; 2002 Aug 06; 33(4):203-8. PubMed ID: 12368991 [Abstract] [Full Text] [Related]
13. Aromatic L-amino acid decarboxylase deficiency: clinical features, drug therapy and follow-up. Manegold C, Hoffmann GF, Degen I, Ikonomidou H, Knust A, Laass MW, Pritsch M, Wilichowski E, Hörster F. J Inherit Metab Dis; 2009 Jun 06; 32(3):371-80. PubMed ID: 19172410 [Abstract] [Full Text] [Related]
14. Simultaneous measurement of monoamine metabolites and 5-methyltetrahydrofolate in the cerebrospinal fluid of children. Akiyama T, Hayashi Y, Hanaoka Y, Shibata T, Akiyama M, Nakamura K, Tsuyusaki Y, Kubota M, Yoshinaga H, Kobayashi K. Clin Chim Acta; 2017 Feb 06; 465():5-10. PubMed ID: 27940130 [Abstract] [Full Text] [Related]
15. Aromatic L-amino acid decarboxylase deficiency: an extrapyramidal movement disorder with oculogyric crises. Korenke GC, Christen HJ, Hyland K, Hunneman DH, Hanefeld F. Eur J Paediatr Neurol; 1997 Feb 06; 1(2-3):67-71. PubMed ID: 10728198 [Abstract] [Full Text] [Related]
16. Abnormal glucose metabolism in aromatic L-amino acid decarboxylase deficiency. Ide S, Sasaki M, Kato M, Shiihara T, Kinoshita S, Takahashi JY, Goto Y. Brain Dev; 2010 Jun 06; 32(6):506-10. PubMed ID: 19520530 [Abstract] [Full Text] [Related]
17. A female case of aromatic l-amino acid decarboxylase deficiency responsive to MAO-B inhibition. Kojima K, Anzai R, Ohba C, Goto T, Miyauchi A, Thöny B, Saitsu H, Matsumoto N, Osaka H, Yamagata T. Brain Dev; 2016 Nov 06; 38(10):959-963. PubMed ID: 27371992 [Abstract] [Full Text] [Related]