300 related articles for article (PubMed ID: 22167275)
1. Long-term outcome and intervention of urea cycle disorders in Japan.
Kido J; Nakamura K; Mitsubuchi H; Ohura T; Takayanagi M; Matsuo M; Yoshino M; Shigematsu Y; Yorifuji T; Kasahara M; Horikawa R; Endo F
J Inherit Metab Dis; 2012 Sep; 35(5):777-85. PubMed ID: 22167275
[TBL] [Abstract][Full Text] [Related]
2. Neurodevelopmental outcome of long-term therapy of urea cycle disorders in Japan.
Uchino T; Endo F; Matsuda I
J Inherit Metab Dis; 1998; 21 Suppl 1():151-9. PubMed ID: 9686352
[TBL] [Abstract][Full Text] [Related]
3. Role of liver transplantation in urea cycle disorders: Report from a nationwide study in Japan.
Kido J; Matsumoto S; Häberle J; Inomata Y; Kasahara M; Sakamoto S; Horikawa R; Tanemura A; Okajima H; Suzuki T; Nakamura K
J Inherit Metab Dis; 2021 Nov; 44(6):1311-1322. PubMed ID: 34232532
[TBL] [Abstract][Full Text] [Related]
4. Clinical manifestations and growth of patients with urea cycle disorders in Japan.
Nakamura K; Kido J; Matsumoto S; Mitsubuchi H; Endo F
J Hum Genet; 2016 Jul; 61(7):613-6. PubMed ID: 26935171
[TBL] [Abstract][Full Text] [Related]
5. Long-term outcome of urea cycle disorders: Report from a nationwide study in Japan.
Kido J; Matsumoto S; Häberle J; Nakajima Y; Wada Y; Mochizuki N; Murayama K; Lee T; Mochizuki H; Watanabe Y; Horikawa R; Kasahara M; Nakamura K
J Inherit Metab Dis; 2021 Jul; 44(4):826-837. PubMed ID: 33840128
[TBL] [Abstract][Full Text] [Related]
6. Early liver transplantation in neonatal-onset and moderate urea cycle disorders may lead to normal neurodevelopment.
Kido J; Matsumoto S; Mitsubuchi H; Endo F; Nakamura K
Metab Brain Dis; 2018 Oct; 33(5):1517-1523. PubMed ID: 29948653
[TBL] [Abstract][Full Text] [Related]
7. Diagnosis and treatment of urea cycle disorder in Japan.
Nakamura K; Kido J; Mitsubuchi H; Endo F
Pediatr Int; 2014 Aug; 56(4):506-9. PubMed ID: 25039902
[TBL] [Abstract][Full Text] [Related]
8. Prenatal treatment of ornithine transcarbamylase deficiency.
Wilnai Y; Blumenfeld YJ; Cusmano K; Hintz SR; Alcorn D; Benitz WE; Berquist WE; Bernstein JA; Castillo RO; Concepcion W; Cowan TM; Cox KL; Lyell DJ; Esquivel CO; Homeyer M; Hudgins L; Hurwitz M; Palma JP; Schelley S; Akula VP; Summar ML; Enns GM
Mol Genet Metab; 2018 Mar; 123(3):297-300. PubMed ID: 29396029
[TBL] [Abstract][Full Text] [Related]
9. Clinical course of 63 patients with neonatal onset urea cycle disorders in the years 2001-2013.
Unsinn C; Das A; Valayannopoulos V; Thimm E; Beblo S; Burlina A; Konstantopoulou V; Mayorandan S; de Lonlay P; Rennecke J; Derbinski J; Hoffmann GF; Häberle J
Orphanet J Rare Dis; 2016 Aug; 11(1):116. PubMed ID: 27538463
[TBL] [Abstract][Full Text] [Related]
10. Cross-sectional observational study of 208 patients with non-classical urea cycle disorders.
Rüegger CM; Lindner M; Ballhausen D; Baumgartner MR; Beblo S; Das A; Gautschi M; Glahn EM; Grünert SC; Hennermann J; Hochuli M; Huemer M; Karall D; Kölker S; Lachmann RH; Lotz-Havla A; Möslinger D; Nuoffer JM; Plecko B; Rutsch F; Santer R; Spiekerkoetter U; Staufner C; Stricker T; Wijburg FA; Williams M; Burgard P; Häberle J
J Inherit Metab Dis; 2014 Jan; 37(1):21-30. PubMed ID: 23780642
[TBL] [Abstract][Full Text] [Related]
11. The role of orotic acid measurement in routine newborn screening for urea cycle disorders.
Staretz-Chacham O; Daas S; Ulanovsky I; Blau A; Rostami N; Saraf-Levy T; Abu Salah N; Anikster Y; Banne E; Dar D; Dumin E; Fattal-Valevski A; Falik-Zaccai T; Hershkovitz E; Josefsberg S; Khammash H; Keidar R; Korman SH; Landau Y; Lerman-Sagie T; Mandel D; Mandel H; Marom R; Morag I; Nadir E; Yosha-Orpaz N; Pode-Shakked B; Pras E; Reznik-Wolf H; Saada A; Segel R; Shaag A; Shaul Lotan N; Spiegel R; Tal G; Vaisid T; Zeharia A; Almashanu S
J Inherit Metab Dis; 2021 May; 44(3):606-617. PubMed ID: 33190319
[TBL] [Abstract][Full Text] [Related]
12. Unusual cause of general malaise: a young woman with ornithine transcarbamylase deficiency.
Singh S; Pal S; Dubrey SW
BMJ Case Rep; 2016 Jan; 2016():. PubMed ID: 26791129
[TBL] [Abstract][Full Text] [Related]
13. Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiency.
Nagasaka H; Yorifuji T; Murayama K; Kubota M; Kurokawa K; Murakami T; Kanazawa M; Takatani T; Ogawa A; Ogawa E; Yamamoto S; Adachi M; Kobayashi K; Takayanagi M
Eur J Pediatr; 2006 Sep; 165(9):618-24. PubMed ID: 16703326
[TBL] [Abstract][Full Text] [Related]
14. Corticosteroid suppresses urea-cycle-related gene expressions in ornithine transcarbamylase deficiency.
Imoto K; Tanaka M; Goya T; Aoyagi T; Takahashi M; Kurokawa M; Tashiro S; Kato M; Kohjima M; Ogawa Y
BMC Gastroenterol; 2022 Mar; 22(1):144. PubMed ID: 35346058
[TBL] [Abstract][Full Text] [Related]
15. The Application of Next-Generation Sequencing (NGS) in Neonatal-Onset Urea Cycle Disorders (UCDs): Clinical Course, Metabolomic Profiling, and Genetic Findings in Nine Chinese Hyperammonemia Patients.
Zhou Q; Huang H; Ma L; Zhu T
Biomed Res Int; 2020; 2020():5690915. PubMed ID: 32934962
[TBL] [Abstract][Full Text] [Related]
16. Neonatal factors related to survival and intellectual and developmental outcome of patients with early-onset urea cycle disorders.
Pontoizeau C; Roda C; Arnoux JB; Vignolo-Diard P; Brassier A; Habarou F; Barbier V; Grisel C; Abi-Warde MT; Boddaert N; Kuster A; Servais A; Kaminska A; Hennequin C; Dupic L; Lesage F; Touati G; Valayannopoulos V; Chadefaux-Vekemans B; Oualha M; Eisermann M; Ottolenghi C; de Lonlay P
Mol Genet Metab; 2020 Jun; 130(2):110-117. PubMed ID: 32273051
[TBL] [Abstract][Full Text] [Related]
17. Citrulline for urea cycle disorders in Japan.
Tanaka K; Nakamura K; Matsumoto S; Kido J; Mitsubuchi H; Ohura T; Endo F
Pediatr Int; 2017 Apr; 59(4):422-426. PubMed ID: 27613354
[TBL] [Abstract][Full Text] [Related]
18. Clinical outcomes of neonatal onset proximal versus distal urea cycle disorders do not differ.
Ah Mew N; Krivitzky L; McCarter R; Batshaw M; Tuchman M;
J Pediatr; 2013 Feb; 162(2):324-9.e1. PubMed ID: 22901741
[TBL] [Abstract][Full Text] [Related]
19. Glycerol phenylbutyrate efficacy and safety from an open label study in pediatric patients under 2 months of age with urea cycle disorders.
Longo N; Diaz GA; Lichter-Konecki U; Schulze A; Inbar-Feigenberg M; Conway RL; Bannick AA; McCandless SE; Zori R; Hainline B; Ah Mew N; Canavan C; Vescio T; Kok T; Porter MH; Berry SA
Mol Genet Metab; 2021 Jan; 132(1):19-26. PubMed ID: 33388234
[TBL] [Abstract][Full Text] [Related]
20. Long-term outcomes in Ornithine Transcarbamylase deficiency: a series of 90 patients.
Brassier A; Gobin S; Arnoux JB; Valayannopoulos V; Habarou F; Kossorotoff M; Servais A; Barbier V; Dubois S; Touati G; Barouki R; Lesage F; Dupic L; Bonnefont JP; Ottolenghi C; De Lonlay P
Orphanet J Rare Dis; 2015 May; 10():58. PubMed ID: 25958381
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
