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Original Article

Primary Hereditary Systemic Amyloidosis (Meretoja's Syndrome): Clinical Features and Treatment by Plastic Surgery

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Pages 141-145 | Received 17 Sep 1987, Published online: 08 Jul 2009

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Read on this site (3)

Maarit Tanskanen, Anders Paetau, Oili Salonen, Tapani Salmi, Antti Lamminen, Perttu Lindsberg, Hannu Somer & Sari Kiuru-Enari. (2009) Withdrawn: Severe ataxia with neuropathy in hereditary gelsolin amyloidosis. Amyloid 16:4, pages 246-246.
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Maarit Tanskanen, Anders Paetau, Oili Salonen, Tapani Salmi, Antti Lamminen, Perttu Lindsberg, Hannu Somer & Sari Kiuru-Enari. (2007) Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: A case report. Amyloid 14:1, pages 89-95.
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Articles from other publishers (8)

Sari Kiuru-Enari & Matti Haltia. 2013. Peripheral Nerve Disorders. Peripheral Nerve Disorders 659 681 .
Tiia Pihlamaa, Jorma Rautio, Sari Kiuru-Enari & Sinikka Suominen. (2011) Gelsolin Amyloidosis as a Cause of Early Aging and Progressive Bilateral Facial Paralysis. Plastic and Reconstructive Surgery 127:6, pages 2342-2351.
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Scott W. Wolfe. 2011. Green's Operative Hand Surgery. Green's Operative Hand Surgery 2067 2088 .
S. Kiuru-Enari, J. Keski-Oja & M. Haltia. (2005) Cutis laxa in hereditary gelsolin amyloidosis. British Journal of Dermatology 152:2, pages 250-257.
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Reijo Norio. (2003) The Finnish disease heritage III: the individual diseases. Human Genetics 112:5-6, pages 470-526.
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Sari Kiuru-Enari, Hannu Somer, Anna-Maria Seppäläinen, Irma-Leena Notkola & Matti Haltia. (2002) Neuromuscular Pathology in Hereditary Gelsolin Amyloidosis. Journal of Neuropathology & Experimental Neurology 61:6, pages 565-571.
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Rabindra A. Braganza, Robert Tien, Henry T. Hoffman & Parviz H. Haghighi. (2009) Amyloid of the facial nerve. The Laryngoscope 102:12, pages 1372-1376.
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Tomy Starck, Kenneth R. Kenyon, Laila A. Hanninen, Charles Beyer-Machule, Richard Fabian, Robert A. Gorn, F. Dickinson McMullan, Jules Baum & Keith P.W.J. McAdam. (1991) Clinical and Histopathologic Studies of Two Families with Lattice Corneal Dystrophy and Familial Systemic Amyloidosis (Meretoja Syndrome). Ophthalmology 98:8, pages 1197-1206.
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