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78 Possible Causes for Stapelia, rufa

  • Aristolochia Petersiana

    Stangea rhizanta Stanhopea tigrina Stanleya albescens Stanleya elata Stanleya pinnatifida Stanleya viridiflora Stanleya wrightii Stapelia kwebensis Stapelia marientalensis[foodplantsinternational.com] […] pennelliana , philoxeroides f. angustifolia , philoxeroides f. philoxeroides , piptantha , porrigens , praelonga var. australis , puberula , pumila , pungens , reineckii , rufa[www2.darwin.edu.ar] […] simplex;Lwejwe;;;/ GRAMINEAE;Brachiaria;brizantha;Mbute;;fr;/ GRAMINEAE;Imperata;cylindrica;Mnyaki;Motomoto;;/ GRAMINEAE;Sorghum;bicolor;Nkonge;;;/ GRAMINEAE;Hyparrhenia;rufa[pages.ucsd.edu]

  • Xanthomatosis

    Dotti MT, Rufa A, Federico A. Cerebrotendinous xanthomatosis: heterogeneity of clinical phenotype with evidence of previously undescribed ophthalmological findings .[disorders.eyes.arizona.edu] […] report. ( 29390551 ) Li D....Tan L. 2017 33 The role of dentate nuclei in human oculomotor control: insights from cerebrotendinous xanthomatosis. ( 28168705 ) Rosini F....Rufa[malacards.org] Dotti MT, Rufa A, Federico A. Cerebrotendinous xanthomatosis: heterogeneity of clinical phenotype with evidence of previously undescribed ophthalmological findings.[rarediseases.org]

    Missing: Stapelia
  • Cerebrotendinous Xanthomatosis

    Dotti MT, Rufa A, Federico A. Cerebrotendinous xanthomatosis: heterogeneity of clinical phenotype with evidence of previously undescribed ophthalmological findings .[disorders.eyes.arizona.edu] Dotti MT, Rufa A, Federico A. Cerebrotendinous xanthomatosis: heterogeneity of clinical phenotype with evidence of previously undescribed ophthalmological findings.[emedicine.medscape.com] Szlago M, Gallus GN, Schenone A, Patiño ME, Sfaelo Z, Rufa A, et al. The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene.[emedicine.medscape.com]

    Missing: Stapelia
  • Sterol 27-Hydroxylase Deficiency

    Dotti MT, Rufa A, Federico A. Cerebrotendinous xanthomatosis: heterogeneity of clinical phenotype with evidence of previously undescribed ophthalmological findings.[rarediseases.org] Szlago M, Gallus GN, Schenone A, Patiño ME, Sfaelo Z, Rufa A, et al. The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene.[emedicine.medscape.com] Dotti MT, Rufa A, Federico A. Cerebrotendinous xanthomatosis: heterogeneity of clinical phenotype with evidence of previously undescribed ophthalmological findings .[disorders.eyes.arizona.edu]

    Missing: Stapelia
  • Primrose Syndrome

    Battisti C, Dotti MT, Cerase A, Rufa A, Sicurelli F, Scarpini C, Federico A. The Primerose syndrome with progressive neurological involvement and cerebral calcification.[rarediseases.info.nih.gov] The Primrose syndrome with progressive neurological involvement and cerebral calcification Battisti, C; Dotti, MT; Cerase, A; Rufa, A; Sicurelli, F; Scarpini, C; Federico,[deepdyve.com]

    Missing: Stapelia
  • CADASIL Syndrome

    Stroke. 2001; 32 :17–21. [ PubMed : 11136908 ] Piccirillo G, Magrì D, Mitra M, Rufa A, Zicari E, Stromillo ML, De Stefano N, Dotti MT.[ncbi.nlm.nih.gov] Rufa A, Guideri F, Acampa M, Cevenini G, Bianchi S, De Stefano N, Stromillo ML, Federico A, Dotti MT.[ghr.nlm.nih.gov] Brain. 2015; 138 :2347–58. [ PubMed : 26063658 ] Vinciguerra C, Rufa A, Bianchi S, Sperduto A, De Santis M, Malandrini A, Dotti MT, Federico A.[ncbi.nlm.nih.gov]

    Missing: Stapelia
  • Oculodentodigital Dysplasia

    Article type: Short Communication Authors: Tumminelli, Gemma a Di Donato, Ilaria a Guida, Valentina b Rufa, Alessandra a De Luca, Alessandro b Federico, Antonio a ; * Affiliations[content.iospress.com]

    Missing: Stapelia
  • Wernicke Encephalopathy

    Author information 1 Dipartimento di Scienze Neurologiche Neurochirurgiche e del Comportamento, Università degli Studi di Siena, Siena, Italy. rufa@unisi.it Abstract Wernicke[ncbi.nlm.nih.gov] Rufa I. Vallone P. Galluzzi G. Coratti F. Franchi F. Giannini C.[link.springer.com] Rufa A, Rosini F, Cerase A, et al. Wernicke encephalopathyafter gastrointestinal surgery for cancer: causes of diagnostic failureor delay.[pancreas.imedpub.com]

    Missing: Stapelia
  • Autosomal Dominant Classic Optic Atrophy

    Formichi P, Radi E, Giorgi E, Gallus GN, Brunetti J, Battisti C, Rufa A, Dotti MT, Franceschini R, Bracci L, Federico A.[ghr.nlm.nih.gov] Hum Mutat. 2015; 36 :20–25. [ PubMed : 25243597 ] Gallus GN, Cardaioli E, Rufa A, Da Pozzo P, Bianchi S, D'Eramo C, Collura M, Tumino M, Pavone L, Federico A.[ncbi.nlm.nih.gov]

    Missing: Stapelia
  • Autosomal Dominant Optic Atrophy

    Formichi P 1 , Radi E 1 , Giorgi E 1 , Gallus GN 1 , Brunetti J 2 , Battisti C 1 , Rufa A 1 , Dotti MT 1 , Franceschini R 1 , Bracci L 2 , Federico A 3 .[ncbi.nlm.nih.gov] Formichi P, Radi E, Giorgi E, Gallus GN, Brunetti J, Battisti C, Rufa A, Dotti MT, Franceschini R, Bracci L, Federico A.[ghr.nlm.nih.gov] Hum Mutat. 2015; 36 :20–25. [ PubMed : 25243597 ] Gallus GN, Cardaioli E, Rufa A, Da Pozzo P, Bianchi S, D'Eramo C, Collura M, Tumino M, Pavone L, Federico A.[ncbi.nlm.nih.gov]

    Missing: Stapelia

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