AAAAAA
Results:
1-7
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Results: 7
Authors:
Benson, MD
Liepnieks, JJ
Yazaki, M
Yamashita, T
Asl, KH
Guenther, B
Kluve-Beckerman, B
Citation: Md. Benson et al., A new human hereditary amyloidosis: The result of a stop-codon mutation inthe apolipoprotein AII gene, GENOMICS, 72(3), 2001, pp. 272-277
Authors:
Afolabi, I
Asl, KH
Nakamura, M
Jacobs, P
Hendrie, H
Benson, MD
Citation: I. Afolabi et al., Transthyretin isoleucine-122 mutation in African and American blacks, AMYLOID, 7(2), 2000, pp. 121-125
Authors:
Nakamura, M
Asl, KH
Benson, MD
Citation: M. Nakamura et al., A novel variant of transthyretin (Gln89Lys) associated with familial amyloidotic polyneuropathy, AMYLOID, 7(1), 2000, pp. 46-50
Authors:
Asl, KH
Liepnieks, JJ
Nakamura, M
Benson, MD
Citation: Kh. Asl et al., Organ-specific (localized) synthesis of Ig light chain amyloid, J IMMUNOL, 162(9), 1999, pp. 5556-5560
Authors:
Asl, KH
Liepnieks, JJ
Nakamura, M
Parker, F
Benson, MD
Citation: Kh. Asl et al., A novel apolipoprotein A-1 variant, Arg173Pro, associated with cardiac andcutaneous amyloidosis, BIOC BIOP R, 257(2), 1999, pp. 584-588
Authors:
Asl, LH
Liepnieks, JJ
Asl, KH
Uemichi, T
Moulin, G
Desjoyaux, E
Loire, R
Delpech, M
Grateau, G
Benson, MD
Citation: Lh. Asl et al., Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1, AM J PATH, 154(1), 1999, pp. 221-227
Authors:
Nakamura, M
Yamashita, T
Ando, Y
Asl, KH
Tashima, K
Ohlsson, PI
Kususe, Y
Benson, MD
Citation: M. Nakamura et al., Identification of a new transthyretin variant (IIe49) in familial amyloidotic polyneuropathy using electrospray ionization mass spectrometry and nonisotopic RNase cleavage assay, HUMAN HERED, 49(4), 1999, pp. 186-189
Risultati:
1-7
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