Lämmle B - Search Results

1

Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency.

Fan X, Kremer Hovinga JA, Shirotani-Ikejima H, Eura Y, Hirai H, Honda S, Kokame K, Taleghani MM, von Krogh AS, Yoshida Y, Fujimura Y, Lämmle B, Miyata T. Fan X, et al. Among authors: lammle b. Int J Hematol. 2016 Mar;103(3):283-91. doi: 10.1007/s12185-015-1933-7. Epub 2016 Feb 1. Int J Hematol. 2016. PMID: 26830967 Free article.

2

Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura.

Furlan M, Robles R, Solenthaler M, Wassmer M, Sandoz P, Lämmle B. Furlan M, et al. Among authors: lammle b. Blood. 1997 May 1;89(9):3097-103. Blood. 1997. PMID: 9129011 Free article.

3

Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura.

Furlan M, Robles R, Solenthaler M, Lämmle B. Furlan M, et al. Among authors: lammle b. Blood. 1998 Apr 15;91(8):2839-46. Blood. 1998. PMID: 9531594 Free article.

4

von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome.

Furlan M, Robles R, Galbusera M, Remuzzi G, Kyrle PA, Brenner B, Krause M, Scharrer I, Aumann V, Mittler U, Solenthaler M, Lämmle B. Furlan M, et al. Among authors: lammle b. N Engl J Med. 1998 Nov 26;339(22):1578-84. doi: 10.1056/NEJM199811263392202. N Engl J Med. 1998. PMID: 9828245 Free article.

5

Deficiency of von Willebrand factor-cleaving protease in familial and acquired thrombotic thrombocytopenic purpura.

Furlan M, Lämmle B. Furlan M, et al. Among authors: lammle b. Baillieres Clin Haematol. 1998 Jun;11(2):509-14. doi: 10.1016/s0950-3536(98)80064-4. Baillieres Clin Haematol. 1998. PMID: 10097823

6

Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura.

Furlan M, Robles R, Morselli B, Sandoz P, Lämmle B. Furlan M, et al. Among authors: lammle b. Thromb Haemost. 1999 Jan;81(1):8-13. Thromb Haemost. 1999. PMID: 10348715

7

Assay of von Willebrand factor (vWF)-cleaving protease based on decreased collagen binding affinity of degraded vWF: a tool for the diagnosis of thrombotic thrombocytopenic purpura (TTP).

Gerritsen HE, Turecek PL, Schwarz HP, Lämmle B, Furlan M. Gerritsen HE, et al. Among authors: lammle b. Thromb Haemost. 1999 Nov;82(5):1386-9. Thromb Haemost. 1999. PMID: 10595623

8

von Willebrand factor in thrombotic thrombocytopenic purpura.

Furlan M, Lämmle B. Furlan M, et al. Among authors: lammle b. Thromb Haemost. 1999 Aug;82(2):592-600. Thromb Haemost. 1999. PMID: 10605756 Review. No abstract available.

9

Splenectomy in thrombotic thrombocytopenic purpura.

Furlan M, Lämmle B. Furlan M, et al. Among authors: lammle b. Am J Hematol. 2000 May;64(1):79. doi: 10.1002/(sici)1096-8652(200005)64:1<79::aid-ajh17>3.0.co;2-f. Am J Hematol. 2000. PMID: 10815796 Free article. No abstract available.

10

Microangiopathic haemolytic anaemia in metastasizing malignant tumours is not associated with a severe deficiency of the von Willebrand factor-cleaving protease.

Fontana S, Gerritsen HE, Kremer Hovinga J, Furlan M, Lämmle B. Fontana S, et al. Among authors: lammle b. Br J Haematol. 2001 Apr;113(1):100-2. doi: 10.1046/j.1365-2141.2001.02704.x. Br J Haematol. 2001. PMID: 11328288 Free article.

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