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406 Possible Causes for ramaswamy

  • Sunburn

    Ramaswami, C. Sears, D. Foster, S. E. Lazic, R. Okabe, A. Benner, B. H. Lee, et al.[web.archive.org]

  • Osteoporosis

    Emily A Vargas and Ramaswami Mahalingam , Perceptions of control and improved psychological, physical, and social functioning in postmenopausal women , Journal of Health Psychology[doi.org]

  • Idiopathic Pulmonary Fibrosis

    M , Panos R , Pantano J , Parambil J , Patel NM , Perea Sánchez RA , Perez RL , Peroš-Golubiĉić T , Piñeiro García Calderón A , Posadas Valay R , Pun Leon LE , Rai NS , Ramaswamy[ncbi.nlm.nih.gov]

  • Tuberculosis

    Ramaswamy, J. M. Musser, and D. L. Williams. 1999 . Phenotypic and genotypic characterization of Mycobacterium africanum isolates from West Africa. J. Clin.[doi.org]

  • Phosphorylase Kinase Deficiency

    Beauchamp NJ, Dalton A, Ramaswami U, et al. Glycogen storage disease type IX: high variability in clinical phenotype. Mol Genet Metab. 2007;92:88-99.[rarediseases.org] GSD IX GSDIX PhK deficiency phosphorylase b kinase deficiency phosphorylase kinase deficiency Beauchamp NJ, Dalton A, Ramaswami U, Niinikoski H, Mention K, Kenny P, Kolho[ghr.nlm.nih.gov] Beauchamp NJ, Dalton A, Ramaswami U, Niinikoski H, Mention K, Kenny P, Kolho KL, Raiman J, Walter J, Treacy E, Tanner S, Sharrard M (2007) Glycogen storage disease type IX[doi.org]

  • Progressive Osseous Heteroplasia

    Robert J Pignolo, 1–3 Girish Ramaswamy, 2,3 John T Fong, 2,3 Eileen M Shore, 2–4 Frederick S Kaplan 1–3 1 Department of Medicine, 2 Department of Orthopaedic Surgery, 3 The[dovepress.com] Pignolo RJ, Ramaswamy G, Fong JT, Shore EM, Kaplan FS. Progressive osseous heteroplasia: diagnosis, treatment, and prognosis.[ghr.nlm.nih.gov] REVIEW ARTICLES Pignolo R, Ramaswamy G, Fong J, Shore E, Kaplan F. Progresssive osseous heteroplasia: diagnosis, treatment, and prognosis.[rarediseases.org]

  • Hypochondroplasia

    JOURNAL ARTICLES Ramaswami U, et al. Genotype and phenotype in hypochondroplasia. J Pediatr. 1998;133:99-102. Rousseau F, et al.[rarediseases.org] Ramaswami U, Rumsby G, Hindmarsh PC, Brook CG: Genotype and phenotype in hypochondroplasia. J Pediatr 1998;133:99-102.[karger.com] Ramaswami U, Hindmarsh PC, Brook CG: Growth hormone therapy in hypochondroplasia. Acta Paediatr Suppl 1999;88:116-117.[karger.com]

  • Medulloblastoma

    Ramaswamy V, Remke M, Bouffet E, Faria CC, Perreault S, Cho YJ et al.[emedicine.medscape.com] Perreault S, Ramaswamy V, Achrol AS, Chao K, Liu TT, Shih D, et al. MRI surrogates for molecular subgroups of medulloblastoma.[emedicine.medscape.com] Remke M, Ramaswamy V, Peacock J, Shih DJ, Koelsche C et al. TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma.[emedicine.medscape.com]

  • Fabry Disease

    , Kopp JB , Kröner J , Linhart A , Martins AM , Matern D , Mehta AB , Mignani R , Najafian B , Narita I , Nicholls K , Obrador GT , Oliveira JP , Pisani A , Politei J , Ramaswami[ncbi.nlm.nih.gov] An Haack K, Hopkin RJ, Mauer M, Najafian B, Scott CR, Shankar SP, Thurberg BL, Tøndel C, Tylki-Szymańska A, Ramaswami U.[ncbi.nlm.nih.gov] Ramaswami, A. Gal and A.[doi.org]

  • Glycogen Storage Disease due to Liver Phosphorylase Kinase Deficiency

    Beauchamp NJ, Dalton A, Ramaswami U, et al. Glycogen storage disease type IX: high variability in clinical phenotype. Mol Genet Metab. 2007;92:88-99.[rarediseases.org] GSD IX GSDIX PhK deficiency phosphorylase b kinase deficiency phosphorylase kinase deficiency Beauchamp NJ, Dalton A, Ramaswami U, Niinikoski H, Mention K, Kenny P, Kolho[ghr.nlm.nih.gov] Beauchamp NJ, Dalton A, Ramaswami U, Niinikoski H, Mention K, Kenny P, Kolho K, Raiman J, Walter J, Treacy E, Tanner S, Sharrard M.[path.upmc.edu]

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