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863 Possible Causes for tada

  • Influenza

    Tada, Y., S. Hongo, Y. Muraki, K. Sugawara, F. Kitame, and K. Nakamura. 1997 . Evolutionary analysis of influenza C virus M genes. Virus Genes 15 : 53 -59.[doi.org] In the tree of the M gene sequences, there were two major branch clusters (previously designated lineages I and II by Tada et al. [ 32 ]), one (lineage I) containing KA176[doi.org]

  • Pneumonia

    Ishiwata T 1, 2 , Ebata T 1 , Iwasawa S 1 , Matsushima J 3 , Ota S 3 , Nakatani Y 3 , Tsushima K 2 , Tada Y 2 , Tatsumi K 2 , Takiguchi Y 1 .[ncbi.nlm.nih.gov]

  • Infectious Mononucleosis

    View Article PubMed PubMed Central Google Scholar Kawanishi M, Tada-Oikawa S, Kawanishi S: Epstein-Barr virus BHRF1 functions downstream of Bid cleavage and upstream of mitochondrial[dx.doi.org]

  • Idiopathic Pulmonary Fibrosis

    Kohei Togami, Kotaro Yamaguchi, Sumio Chono and Hitoshi Tada , Evaluation of permeability alteration and epithelial–mesenchymal transition induced by transforming growth factor-β[doi.org] Tomioka H , Kuwata Y , Imanaka K , Hashimoto K , Ohnishi H , Tada K , Sakamoto H , Iwasaki H .[doi.org]

  • Adrenal Insufficiency

    Gut 52 : 1194 –1199, 2003 Inoue T, Ohnishi A, Matsuo A, Kawai B, Kunihiro N, Tada Y, Koizumi F, Chau T, Okada Y, Yamamura Y, Tanaka T: Therapeutic and diagnostic potential[doi.org]

  • Atypical Glycine Encephalopathy

    Baumgartner et al 1969 ; Tada et al 1969 ).[medlink.com] Dev Med ChildNeurol 2002;44:71220.[11] Hayasaka K, Tada K, Fueki N, Nakamura Y, Nyhan WL,Schmidt K, et al.[documents.tips] Kure S, Narisawa K, Tada K (1992) Enzymatic diagnosis of non ketotic hyperglycinemia with lymphoblasts. J Pediatr 120:95–98 PubMed CrossRef Google Scholar 30.[link.springer.com]

  • Glycogen Storage Disease due to Glucose-6-Phosphat Transport Defect

    Chem. 255 (1980) 8381–8384 PubMed Google Scholar Narisawa, K., Igarashi, Y., Otomo, H. and Tada, K.[link.springer.com] Narisawa K, Igarashi Y, Otomo H, Tada K (1978) A new variant of glycogen storage disease type I, probably due to a defect in the glucose-6-phosphate transport system.[springerlink.com] Narisawa K, Igarashi Y, Tada K. Enzyme. 1987;38(1-4):177-83.[humpath.com]

  • Iminoglycinuria

    ., MIZUNO, K. and TADA, K. Atypical Gyrate Atrophy of the Choroid and Retina and Iminoglycinuria . Tohoku J. exp.[doi.org] ., Tada, K., Ando, T., Yoshida, T., Yokoyama, Y., Arakawa, T.: Prolinuria: defect in intestinal absoption of imino acids and glycine. Tohoku J. exp.[springerlink.com] Tada K et. al. (1965) Prolinuria: a new renal tubular defect in transport of proline and glycine. [ ] 10.[moldiag.com]

  • Valinemia

    Tada K, Wada Y, Arakawa T (1967). "Hypervalinemia. Its metabolic lesion and therapeutic approach". Am. J. Dis. Child. 113 (1): 64–7. PMID 6066688.[bionity.com] Tada K, Wada Y, Arakawa T (1967). "Hypervalinemia. Its metabolic lesion and therapeutic approach". Am. J. Dis. Child . 113 (1): 64–67. PMID 6066688 .[wikidoc.org] References Dancis J, Hutzler J, Tada K, Wada Y, Morikawa T, Arakawa T (1967). "Hypervalinemia. A defect in valine transamination". Pediatrics 39 (6): 813–7.[bionity.com]

  • Oculocutaneous Albinism Type 4

    . , Tada J. , Kikuchi N. , Takata M. , Takamori K. , Kishibe M. , Tanaka M. , Miyamura Y. , Ito S. , Tomita Y.[uniprot.org] Inagaki K, Suzuki T, Shimizu H, Ishii N, Umezawa Y, Tada J, Kikuchi N, Takata M, Takamori K, Kishibe M, Tanaka M, Miyamura Y, Ito S, Tomita Y.[disorders.eyes.arizona.edu] . , Tada, J. et al . Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan . Am. J. Hum. Genet. 74 , 466–471 (2004). 21. Costin, G.[nature.com]

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