-
1
-
-
55949124238
-
Factor VII deficiency: defining the clinical picture and optimizing therapeutic options
-
PMid:19141157
-
Lapecorella M, Mariani G. Factor VII deficiency: defining the clinical picture and optimizing therapeutic options. Haemophilia. 2008; 14: 1170-75. http://dx.doi.org/10.1111/j.1365-2516.2008.01844.x PMid:19141157
-
(2008)
Haemophilia
, vol.14
, pp. 1170-1175
-
-
Lapecorella, M.1
Mariani, G.2
-
3
-
-
22544446737
-
Spectrum of inherited bleeding disorders in Indians
-
PMid:16015418
-
Gupta M, Bhattacharyya M, Choudhry VP, Saxena R. Spectrum of inherited bleeding disorders in Indians. Clin Appl Thromb Hemost. 2005; 11: 325-30. http://dx.doi.org/10.1177/107602960501100311 PMid:16015418
-
(2005)
Clin Appl Thromb Hemost.
, vol.11
, pp. 325-330
-
-
Gupta, M.1
Bhattacharyya, M.2
Choudhry, V.P.3
Saxena, R.4
-
4
-
-
41749104247
-
Inherited platelet function disorders versus other inherited bleeding disorders: An Indian overview
-
PMid:17850851
-
Ahmad F, Kannan M, Ranjan R, Bajaj J, Choudhary VP, Saxena R. Inherited platelet function disorders versus other inherited bleeding disorders: An Indian overview. Thrombo Res. 2008; 121: 835-41. http://dx.doi.org/10.1016/j.thromres.2007.07.015 PMid:17850851
-
(2008)
Thrombo Res.
, vol.121
, pp. 835-841
-
-
Ahmad, F.1
Kannan, M.2
Ranjan, R.3
Bajaj, J.4
Choudhary, V.P.5
Saxena, R.6
-
5
-
-
0030669247
-
Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency
-
Peyvandi F, Mannucci PM, Asti D, Abdoullahi M, Di Rocco N, Sharifian R. Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency. Haemophilia. 1997; 3: 242-46. http://dx.doi.org/10.1046/j.1365-2516.1997.00137.x
-
(1997)
Haemophilia.
, vol.3
, pp. 242-246
-
-
Peyvandi, F.1
Mannucci, P.M.2
Asti, D.3
Abdoullahi, M.4
Di Rocco, N.5
Sharifian, R.6
-
6
-
-
4444364103
-
Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias
-
PMid:14995986
-
Acharya SS, Coughlin A, Dimichele DM. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost. 2004; 2: 248-56. http://dx.doi.org/10.1111/j.1538-7836.2003.t01-1-00553.x PMid:14995986
-
(2004)
J Thromb Haemost.
, vol.2
, pp. 248-256
-
-
Acharya, S.S.1
Coughlin, A.2
Dimichele, D.M.3
-
7
-
-
4444269047
-
Recessively inherited coagulation disorders
-
PMid:15138162
-
Mannucci PM, Duga S, Peyvandi F. Recessively inherited coagulation disorders. Blood. 2004; 104: 1243-52. http://dx.doi.org/10.1182/blood-2004-02-0595 PMid:15138162
-
(2004)
Blood.
, vol.104
, pp. 1243-1252
-
-
Mannucci, P.M.1
Duga, S.2
Peyvandi, F.3
-
8
-
-
84860343155
-
Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India
-
PMid:22221743
-
Viswabandya A, Baidya S, Nair SC, Abraham A, George B, Mathews V, Chandy M, Srivastava A.Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India. Haemophilia. 2012;18:195-200. http://dx.doi.org/10.1111/j.1365-2516.2011.02730.x PMid:22221743
-
(2012)
Haemophilia.
, vol.18
, pp. 195-200
-
-
Viswabandya, A.1
Baidya, S.2
Nair, S.C.3
Abraham, A.4
George, B.5
Mathews, V.6
Chandy, M.7
Srivastava, A.8
-
9
-
-
0031848372
-
Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients
-
PMid:9695984
-
Peyvandi F, Mannucci PM, Lak M, Abdoullahi M, Zeinali S, Sharifian R, et al. Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients. Brit J haematol. 1998; 102: 626-28. http://dx.doi.org/10.1046/j.1365-2141.1998.00806.x PMid:9695984
-
(1998)
Brit J haematol.
, vol.102
, pp. 626-628
-
-
Peyvandi, F.1
Mannucci, P.M.2
Lak, M.3
Abdoullahi, M.4
Zeinali, S.5
Sharifian, R.6
-
10
-
-
33747168208
-
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene
-
PMid:16919077
-
Herrmann FH, Auerswald G, Ruiz-Saez A, Navarrete M, Pollmann H, Lopaciuk S. Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene. Haemophilia. 2006; 12: 479-89. http://dx.doi.org/10.1111/j.1365-2516.2006.01303.x PMid:16919077
-
(2006)
Haemophilia.
, vol.12
, pp. 479-489
-
-
Herrmann, F.H.1
Auerswald, G.2
Ruiz-Saez, A.3
Navarrete, M.4
Pollmann, H.5
Lopaciuk, S.6
-
11
-
-
51249109038
-
Intracranial haemorrhage in patients with congenital haemostatic defects
-
PMid:18637845
-
Mishra P, Naithani R, Dolai T, Bhargava R, Mahapatra M, Dixit A. Intracranial haemorrhage in patients with congenital haemostatic defects. Haemophilia. 2008; 14: 952-55. http://dx.doi.org/10.1111/j.1365-2516.2008.01814.x PMid:18637845
-
(2008)
Haemophilia.
, vol.14
, pp. 952-955
-
-
Mishra, P.1
Naithani, R.2
Dolai, T.3
Bhargava, R.4
Mahapatra, M.5
Dixit, A.6
-
12
-
-
27544483109
-
Clinico-hematologic profile of factor XIII-deficient patients
-
PMid:16244775
-
Bhattacharya M, Biswas A, Ahmed RPH, Kannan M, Gupta M, Mahapatra M. Clinico-hematologic profile of factor XIII-deficient patients. Clin Appl Thromb Hemost. 2005; 11: 475-80. http://dx.doi.org/10.1177/107602960501100416 PMid:16244775
-
(2005)
Clin Appl Thromb Hemost.
, vol.11
, pp. 475-480
-
-
Bhattacharya, M.1
Biswas, A.2
Ahmed, R.P.H.3
Kannan, M.4
Gupta, M.5
Mahapatra, M.6
-
13
-
-
2142649140
-
Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency
-
PMid:12911609
-
Lak M, Peyvandi F, Ali Sharifian A, Karimi K, Mannucci PM. Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency. J Thromb Haemost. 2003; 1: 1852-53. http://dx.doi.org/10.1046/j.1538-7836.2003.00338.x PMid:12911609
-
(2003)
J Thromb Haemost.
, vol.1
, pp. 1852-1853
-
-
Lak, M.1
Peyvandi, F.2
Ali Sharifian, A.3
Karimi, K.4
Mannucci, P.M.5
-
14
-
-
84859178756
-
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders
-
PMid:22321862
-
Peyvandi F, Palla R, Menegatti M, Siboni SM, et al. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders. J Thromb Haemost. 2012;10: 615-21. http://dx.doi.org/10.1111/j.1538-7836.2012.04653.x PMid:22321862
-
(2012)
J Thromb Haemost.
, vol.10
, pp. 615-621
-
-
Peyvandi, F.1
Palla, R.2
Menegatti, M.3
Siboni, S.M.4
-
15
-
-
0031876281
-
Clinical picture and treatment strategies in factor VII deficiency
-
PMid:9873815
-
Lee CA, Kessler CM, Varon D, Martinowitz U, Heim M. Clinical picture and treatment strategies in factor VII deficiency. Haemophilia. 1998; 4: 689-96. http://dx.doi.org/10.1046/j.1365-2516.1998.440689.x PMid:9873815
-
(1998)
Haemophilia.
, vol.4
, pp. 689-696
-
-
Lee, C.A.1
Kessler, C.M.2
Varon, D.3
Martinowitz, U.4
Heim, M.5
-
16
-
-
84355166767
-
Central nervous system bleeding in patients with rare bleeding disorders
-
PMid:21539694
-
Siboni SM, Zanon E, Sottilotta G, Consonni D, Castaman G, et al. Central nervous system bleeding in patients with rare bleeding disorders. Haemophilia. 2012;18: 34-8. http://dx.doi.org/10.1111/j.1365-2516.2011.02545.x PMid:21539694
-
(2012)
Haemophilia.
, vol.18
, pp. 34-38
-
-
Siboni, S.M.1
Zanon, E.2
Sottilotta, G.3
Consonni, D.4
Castaman, G.5
-
17
-
-
33745232327
-
Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia
-
PMid:16839371
-
Peyvandi F, Haertel S, Knaub S, Mannucci PM. Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia. J Thromb Haemost. 2006; 4: 1634-37. http://dx.doi.org/10.1111/j.1538-7836.2006.02014.x PMid:16839371
-
(2006)
J Thromb Haemost.
, vol.4
, pp. 1634-1637
-
-
Peyvandi, F.1
Haertel, S.2
Knaub, S.3
Mannucci, P.M.4
-
18
-
-
0036588699
-
Rare coagulation deficiencies
-
PMid:12010428
-
Peyvandi F, Duga S, Akhavan S, Mannucci PM. Rare coagulation deficiencies. Haemophilia. 2002; 8: 308-21. http://dx.doi.org/10.1046/j.1365-2516.2002.00633.x PMid:12010428
-
(2002)
Haemophilia.
, vol.8
, pp. 308-321
-
-
Peyvandi, F.1
Duga, S.2
Akhavan, S.3
Mannucci, P.M.4
-
19
-
-
56049098385
-
Rare inherited disorders of fibrinogen
-
PMid:19141154
-
Acharya SS, Dimichele DM. Rare inherited disorders of fibrinogen. Haemophilia. 2008; 14: 1151-58. http://dx.doi.org/10.1111/j.1365-2516.2008.01831.x PMid:19141154
-
(2008)
Haemophilia.
, vol.14
, pp. 1151-1158
-
-
Acharya, S.S.1
Dimichele, D.M.2
-
20
-
-
0343603909
-
Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia
-
PMid:10520042
-
Lak M, Keihani M, Elahi F, Peyvandi F, Mannucci PM. Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia. Brit J haematol. 1999; 107: 204-6. http://dx.doi.org/10.1046/j.1365-2141.1999.01681.x PMid:10520042
-
(1999)
Brit J haematol.
, vol.107
, pp. 204-206
-
-
Lak, M.1
Keihani, M.2
Elahi, F.3
Peyvandi, F.4
Mannucci, P.M.5
-
21
-
-
0036096074
-
Factor XI deficiency in Iranians: its clinical manifestations in comparison with those of classic hemophilia
-
PMid:12010665
-
Peyvandi F, Lak M, Mannucci PM. Factor XI deficiency in Iranians: its clinical manifestations in comparison with those of classic hemophilia. Haematologica. 2002; 87: 512-14. PMid:12010665
-
(2002)
Haematologica.
, vol.87
, pp. 512-514
-
-
Peyvandi, F.1
Lak, M.2
Mannucci, P.M.3
-
22
-
-
0031881892
-
Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII
-
PMid:9531348
-
Peyvandi F, Tuddenham EGD, Akhtari AM, Lak M, Mannucci PM. Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII. Brit J Haematol. 1998; 100: 733-34. http://dx.doi.org/10.1046/j.1365-2141.1998.00620.x PMid:9531348
-
(1998)
Brit J Haematol.
, vol.100
, pp. 733-734
-
-
Peyvandi, F.1
Tuddenham, E.G.D.2
Akhtari, A.M.3
Lak, M.4
Mannucci, P.M.5
-
23
-
-
0033824690
-
Combined factor V and VIII deficiency in Indian population
-
PMid:11012693
-
Shetty S, Madkaikar M, Nair S, Pawar A, Baindur S, Pathare A. Combined factor V and VIII deficiency in Indian population. Haemophilia. 2000; 6: 504-7. http://dx.doi.org/10.1046/j.1365-2516.2000.00421.x PMid:11012693
-
(2000)
Haemophilia.
, vol.6
, pp. 504-507
-
-
Shetty, S.1
Madkaikar, M.2
Nair, S.3
Pawar, A.4
Baindur, S.5
Pathare, A.6
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