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A new Indian family affected by gelsolin amyloidosis

Maramattom Boby Varkey, Chickabasaviah Yasha T

Year : 2013| Volume: 61| Issue : 6 | Page no: 673-675

   This article has been cited by
1 Hearing problems in patients with hereditary gelsolin amyloidosis
Tuuli Mustonen, Ville Sivonen, Sari Atula, Sari Kiuru-Enari, Saku T. Sinkkonen
Orphanet Journal of Rare Diseases. 2021; 16(1)
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2 The role of gelsolin domain 3 in familial amyloidosis (Finnish type)
Habiba Zorgati, Mårten Larsson, Weitong Ren, Adelene Y. L. Sim, Jan Gettemans, Jonathan M. Grimes, Wenfei Li, Robert C. Robinson
Proceedings of the National Academy of Sciences. 2019; 116(28): 13958
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3 Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families
Tuuli Mustonen,Eeva-Kaisa Schmidt,Miko Valori,Pentti J Tienari,Sari Atula,Sari Kiuru-Enari
European Journal of Human Genetics. 2018; 26(1): 117
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4 The First Argentinian Family with Familial Amyloidosis of the Finnish Type
Francisco Lucero Saá,Federico Andrés Cremona,Natalia Ximena Mínguez,María Laura Igarzabal,Pablo Chiaradía
Case Reports in Ophthalmology. 2017; 8(2): 446
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5 Causes of death and life span in Finnish gelsolin amyloidosis
Eeva-Kaisa Schmidt,Sari Atula,Maarit Tanskanen,Tuuli Nikoskinen,Irma-Leena Notkola,Sari Kiuru-Enari
Annals of Medicine. 2016; 48(5): 352
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6 Progressive cranial nerve involvement and grading of facial paralysis in gelsolin amyloidosis
Tiia Pihlamaa,Tapani Salmi,Sinikka Suominen,Sari Kiuru-Enari
Muscle & Nerve. 2016; 53(5): 762
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7 Natural course of Finnish gelsolin amyloidosis
Tuuli Nikoskinen,Eeva-Kaisa Schmidt,Daniel Strbian,Sari Kiuru-Enari,Sari Atula
Annals of Medicine. 2015; 47(6): 506
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8 Penetrating Keratoplasty for Corneal Amyloidosis in Familial Amyloidosis, Finnish Type
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Ophthalmology. 2014;
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