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171 Possible Causes for rafi

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  • Dementia

    Fitzpatrick, Caroline Gardner, Daisy M Gaunt, Bruce Guthrie, Sandra Hollinghurst, Bryar Kadir, Victoria Lee, John McLeod, Stewart W Mercer, Keith R Moffat, Emma Moody, Imran Rafi[doi.org]

  • Tuberculosis

    Rafi, A., M. Spigelman, J. Stanford, E. Lemma, H. Donoghue, and J. Zias. 1994 . Mycobacterium leprae DNA from ancient bone detected by PCR. Lancet 343 : 1360 -1361.[dx.doi.org] ., Rafi, W., Cheruvu, M., Powell, K. R., Zaunbrecher, M. A., Bornmann, W., et al. (2012).[dx.doi.org]

  • Globoid Cell Leukodystrophy

    Wenger DA, Luzi P, Rafi MA.[ncbi.nlm.nih.gov] Rafi, Paola Luzi, Joel Zlotogora and David A.[doi.org] Hum Mutat. 2007; 28 :742. [ PubMed : 17579360 ] Luzi P, Rafi MA, Wenger DA.[ncbi.nlm.nih.gov]

  • Hallopeau Siemens Disease

    Recessive Dystrophic EB – Rafi’s Diagnosis In Rafi’s case, her body, before transplant, did not produce Collagen 7, the primary building block of something called anchoring[rafisrun.com] In short, Rafi got two bad copies of the gene, thus resulting in a much more severe form.[rafisrun.com] Rafi does not have those latches, or anchoring fibrils and thus her two layers of skin are unable to bind together.[rafisrun.com]

  • Epidermolysis Bullosa

    Recessive Dystrophic EB – Rafi’s Diagnosis In Rafi’s case, her body, before transplant, did not produce Collagen 7, the primary building block of something called anchoring[rafisrun.com] […] next 6-year-old Rafi on the beach. Rafi suffers from epidermolysis bullosa, a condition that causes her skin to blister when she encounters trauma.[foxnews.com] […] debra of America Video: Rafi’s Story —It Won’t Hurt to Watch This is Rafi Lily’s story, who is living with Epidermolysis Bullosa (EB), a rare and life-threatening skin disorder[fibrocell.com]

  • Atypical Krabbe Disease due to Saposin A Deficiency

    Luzi P, Rafi MA, Wenger DA: Structure and organization of the human galactocerebrosidase ( GALC ) gene. Genomics 1995;26:407-409 4.[mayomedicallaboratories.com] Luzi P, Rafi MA, Wenger DA: Characterization of the large deletion in the GALC gene found in patients with Krabbe disease. Hum Mol Genet 1995;4(12):2335-2338 5.[mayomedicallaboratories.com]

  • Pyramidal Tract Disorder

    Luzi P, Rafi MA, Wenger DA. Multiple mutations in the GALC gene in a patient with adult-onset Krabbe disease. Ann Neurol 1996;40:116–119.[link.springer.com] References Wenger DA, Rafi MA, Luzi P. Molecular genetics of Krabbe disease (globoid cell leukodystrophy): diagnostic and clinical implications.[ajnr.org] Wenger DA, Rafi MA, Luzi P. Molecular genetics of Krabbe disease (Globoid cell leukodystrophy): diagnostic and clinical implications. Hum Mutat 1997;10:268–279.[link.springer.com]

  • Factor VIII Antibody

    Schwarz (1, 2) , Rafi U. Ahmad (2) , Peter L. Turecek (2) , Friedrich Dorner (2) , Birgit M.[th.schattauer.de]

  • Dystrophic Epidermolysis Bullosa

    Recessive Dystrophic EB – Rafi’s Diagnosis In Rafi’s case, her body, before transplant, did not produce Collagen 7, the primary building block of something called anchoring[rafisrun.com] In short, Rafi got two bad copies of the gene, thus resulting in a much more severe form.[rafisrun.com] Rafi does not have those latches, or anchoring fibrils and thus her two layers of skin are unable to bind together.[rafisrun.com]

  • TORCH Syndrome

    Junaid Rafi , Re: Utility of routine urine CMV PCR and total serum IgM testing of small for gestational age infants: a single center review , Journal of Perinatal Medicine[dx.doi.org] Junaid Rafi and Haroona Khalil , Re: Polyhydramnios in singleton pregnancies: perinatal outcomes and management , The Obstetrician & Gynaecologist , 17 , 1 , (68-69) , (2015[dx.doi.org] Humera Fayyaz and Junaid Rafi , TORCH screening in polyhydramnios: an observational study , The Journal of Maternal-Fetal & Neonatal Medicine , 25 , 7 , (1069) , (2012) .[dx.doi.org]

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