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918 Possible Causes for lois

  • Endocrine Dysfunction

    Authors: Rachel Pollack Lois Jovanovič Hardcover ISBN: 9781455779826 eBook ISBN: 9781455709175 Published Date: 3rd January 2012 Secure Checkout Personal information is secured[elsevier.com] 3rd January 2012 Imprint: Saunders Hardcover ISBN: 9781455779826 eBook ISBN: 9781455709175 Rachel Pollack Author Affiliations and Expertise Mount Sinai School of Medicine Lois[elsevier.com]

  • Meningitis

    Loy ST, Tan CW. Granulomatous meningitis. Singap Med J. 2009;50:371–3. 12. Pai S, Welsh CT, Patel S, Rumboldt Z.[springermedizin.de]

  • Dementia

    Archived from the original on 2016-05-03. a b Loy CT, Schofield PR, Turner AM, Kwok JB (March 2014). "Genetics of dementia".[en.wikipedia.org]

  • Elastoderma

    ., Lois Y. Matsuoka, M.D., and Jouni Uitto, M.D., Ph.D. This article has no abstract; the first 100 words appear below.[nejm.org]

  • Erosive Pustular Dermatosis of the Scalp

    Erosive pustular dermatosis of the scalp: Clinical, trichoscopic, and histopathologic features of 20 cases Michela Starace, Camilla Loi, Francesca Bruni, Aurora Alessandrini[scilit.net] Adv Biomed Res 2 Erosive pustular dermatosis of the scalp: Clinical, trichoscopic, and histopathologic features of 20 cases Michela Starace,Camilla Loi,Francesca Bruni,Aurora[advbiores.net]

  • Idarubicin

    N. de Graaf, Lois W. Dow, John H. Rodman, William E. Evans, Bruce S. Alpert and Sharon B. Murphy.[apexbt.com]

  • Congenital Mesoblastic Nephroma

    We found no LOI in two cellular or mixed type tumors or in two classical type tumors, and concluded that the role of the LOI of IGF2 is not essential for the development and[ncbi.nlm.nih.gov] To clarify whether IGF2, a paternally expressed gene on chromosome 11, has a certain role in the tumorigenic process of CMN through a loss of imprinting (LOI), we studied[ncbi.nlm.nih.gov]

  • Pyrimethamine

    We are indebted to the Misses Le Teng Go, Lois Brenner and Leona Bändel for technical assistance and to Dr. Irving Leopold for allowing us to study and report the case.[nejm.org]

  • Glaucoma - Sleep Apnea Syndrome

    Alon Harris, MS, PhD, FARVO Director of Clinical Research Lois Letzter Professor of Ophthalmology Professor of Cellular and Integrative Physiology[books.google.com]

  • Pseudohypoparathyroidism Type 1B

    Most patients with pseudohypoparathyroidism type 1b (PHP-1b) display a loss of imprinting (LOI) encompassing the GNAS locus resulting in PTH resistance.[ncbi.nlm.nih.gov] In other imprinting disorders, such as Russell-Silver or Beckwith-Wiedemann syndrome, we and others have shown that the LOI is not restricted to one imprinted locus but may[ncbi.nlm.nih.gov] We found multilocus imprinting defects in four PHP-1b patients carrying broad LOI at the GNAS locus (1) simultaneous hypermethylation at L3MBTL1 differentially methylated[ncbi.nlm.nih.gov]

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