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51

Evolution of Haemophilia Care in Europe: 10 years of the principles of care

Noone, D., OâMahony, B., Peyvandi, F., Makris, M., Bok, A.

Journal:

Orphanet Journal of Rare Diseases

Year:

2020

File:

PDF, 1.23 MB

2020

52

The assessment of electromagnetic fields-caused genetic diversity of Tea Camellia sinensis L. using ISSR and SCoT markers

Azizi, Seyed Mohammad Yousef, Hosseini Sarghein, Siavash, Majd, Ahmad, Peyvandi, Maryam

Journal:

Brazilian Journal of Botany

Year:

2020

File:

PDF, 2.35 MB

2020

53

X Chromosome inactivation: a modifier of factor VIII and IX plasma levels and bleeding phenotype in Haemophilia carriers

Garagiola, Isabella, Mortarino, Mimosa, Siboni, Simona Maria, Boscarino, Marco, Mancuso, Maria Elisa, Biganzoli, Marina, Santagostino, Elena, Peyvandi, Flora

Journal:

European Journal of Human Genetics

Year:

2020

File:

PDF, 589 KB

2020

54

A rare inherited coagulation disorder: Combined homozygous factor VII and factor X deficiency

Marzia Menegatti, Mehran Karimi, Isabella Garagiola, PierMannuccio Mannucci, Flora Peyvandi

Journal:

American Journal of Hematology

Year:

2004

Language:

english

File:

PDF, 47 KB

english, 2004

55

Presentation and pattern of symptoms in 382 patients with Glanzmann thrombasthenia in Iran

G. Toogeh, R. Sharifian, M. Lak, R. Safaee, A. Artoni, F. Peyvandi

Journal:

American Journal of Hematology

Year:

2004

Language:

english

File:

PDF, 48 KB

english, 2004

56

Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII

Dipika Mohanty, Kanjaksha Ghosh, Shrimati Shetty, Marta Spreafico, Isabella Garagiola, Flora Peyvandi

Journal:

American Journal of Hematology

Year:

2005

Language:

english

File:

PDF, 65 KB

english, 2005

57

Initial experience from a double-blind, placebo-controlled, clinical outcome study of ARC1779 in patients with thrombotic thrombocytopenic purpura

Spero R. Cataland, Flora Peyvandi, Pier M. Mannucci, Bernhard Lämmle, Johanna A. Kremer Hovinga, Samuel J. Machin, Marie Scully, Gail Rock, James C. Gilbert, Shangbin Yang, Haifeng Wu, Bernd Jilma, Pa

Journal:

American Journal of Hematology

Year:

2012

Language:

english

File:

PDF, 746 KB

english, 2012

58

The total colorant sensitivity of a color matching recipe: An approach to colorant weighting and tinctorial strength errors

Shahram Peyvandi, Seyed Hossein Amirshahi, Boris Sluban

Journal:

Color Research & Application

Year:

2008

Language:

english

File:

PDF, 125 KB

english, 2008

59

Paramerism and reliable parameric correction

Shahram Peyvandi, Seyed Hossein Amirshahi

Journal:

Color Research & Application

Year:

2011

Language:

english

File:

PDF, 2.13 MB

english, 2011

60

Role of the 2 adenine (g.11293_11294insAA) insertion polymorphism in the 3′ untranslated region of the factor VII (FVII) gene: molecular characterization of a patient with severe FVII deficiency

F. Peyvandi, I. Garagiola, R. Palla, N. Marziliano, P. M. Mannucci

Journal:

Year:

2005

Language:

english

File:

PDF, 330 KB

english, 2005

61

Mechanisms of the interaction between two ADAMTS13 gene mutations leading to severe deficiency of enzymatic activity

Flora Peyvandi, Silvia Lavoretano, Roberta Palla, Carla Valsecchi, Giuliana Merati, Raimondo De Cristofaro, Edoardo Rossi, Pier Mannuccio Mannucci

Journal:

Year:

2006

Language:

english

File:

PDF, 312 KB

english, 2006

62

ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura

Luca A. Lotta, Isabella Garagiola, Roberta Palla, Andrea Cairo, Flora Peyvandi

Journal:

Year:

2010

Language:

english

File:

PDF, 223 KB

english, 2010

63

Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency

Flora Peyvandi, Liliana Tagliabue, Marzia Menegatti, Mehran Karimi, Istvan Komáromi, Éva Katona, Laszlo Muszbek, Pier Mannuccio Mannucci

Journal:

Year:

2004

Language:

english

File:

PDF, 149 KB

english, 2004

64

CYP2C9 genotypes and dose requirements during the induction phase of oral anticoagulant therapy

Journal:

Clinical Pharmacology & Therapeutics

Year:

2004

Language:

english

File:

PDF, 176 KB

english, 2004

65

Modeling of volatile organic compounds removal from water by pervaporation process

A.A. Ghoreyshi, M. Jahanshahi, K. Peyvandi

Journal:

Year:

2008

Language:

english

File:

PDF, 230 KB

english, 2008

66

Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII

Peyvandi, Tuddenham, Akhtari, Lak, Mannucci

Journal:

British Journal of Haematology

Year:

1998

Language:

english

File:

PDF, 246 KB

english, 1998

67

Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients

Peyvandi, Mannucci, Lak, Abdoullahi, Zeinali, Sharifian, Perry

Journal:

British Journal of Haematology

Year:

1998

Language:

english

File:

PDF, 223 KB

english, 1998

68

Symptoms of inherited factor V deficiency in 35 Iranian patients

Lak, Sharifian, Peyvandi, Mannucci

Journal:

British Journal of Haematology

Year:

1998

Language:

english

File:

PDF, 66 KB

english, 1998

69

Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia

Lak, Keihani, Elahi, Peyvandi, Mannucci

Journal:

British Journal of Haematology

Year:

1999

Language:

english

File:

PDF, 50 KB

english, 1999

70

A novel polymorphism in intron 1a of the human factor VII gene (G73A): study of a healthy Italian population and of 190 young survivors of myocardial infarction

Peyvandi, Mannucci, Bucciarelli, Zeinali, Akhavan, Sacchi, Merlini, Perry

Journal:

British Journal of Haematology

Year:

2000

Language:

english

File:

PDF, 92 KB

english, 2000

71

Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency

Flora Peyvandi, Marzia Menegatti, Elena Santagostino, Sepideh Akhavan, James Uprichard, David J. Perry, Stephen J. Perkins, Pier M. Mannucci

Journal:

British Journal of Haematology

Year:

2002

Language:

english

File:

PDF, 318 KB

english, 2002

72

Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency

F. PEYVANDI, P. M. MANNUCCI, D. ASTI, M. ABDOULLAHI, N. DI ROCCO, R. SHARIFIAN

Journal:

Year:

1997

Language:

english

File:

PDF, 148 KB

english, 1997

73

Rare coagulation deficiencies

F. Peyvandi, S. Duga, S. Akhavan, P. M. Mannucci

Journal:

Year:

2002

Language:

english

File:

PDF, 717 KB

english, 2002

74

Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domain

R. Asselta, M. C. Montefusco, S. Duga, M. Malcovati, F. Peyvandi, P. M. Mannucci, M. L. Tenchini

Journal:

Journal of Thrombosis and Haemostasis

Year:

2003

Language:

english

File:

PDF, 183 KB

english, 2003

75

Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency

M. Lak, F. Peyvandi, A. Ali Sharifian, K. Karimi, P. M. Mannucci

Journal:

Journal of Thrombosis and Haemostasis

Year:

2003

Language:

english

File:

PDF, 354 KB

english, 2003

76

Warfarin and acenocoumarol dose requirements according to CYP2C9 genotyping in North-Italian patients

M. Spreafico, F. Peyvandi, D. Pizzotti, M. Moia, P. M. Mannucci

Journal:

Journal of Thrombosis and Haemostasis

Year:

2003

Language:

english

File:

PDF, 282 KB

english, 2003

77

Spontaneous splenic rupture in a patient with factor XIII deficiency and a novel mutation

Hassan Khalife, Samar Muwakkit, Hayfa Al-Moussawi, Ibrahim Dabbous, Ruby Khoury, Flora Peyvandi, Miguel R. Abboud

Journal:

Pediatric Blood & Cancer

Year:

2008

Language:

english

File:

PDF, 70 KB

english, 2008

78

Pitfalls in molecular diagnosis in a family with severe factor VII (FVII) deficiency—misdiagnosis by direct sequence analysis using a PCR product

Isabella Garagiola, Roberta Palla, Flora Peyvandi

Journal:

Prenatal Diagnosis

Year:

2003

Language:

english

File:

PDF, 119 KB

english, 2003

79

Clinical and laboratory patterns of the haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura in southern Iran

Mehran Karimi, Ameneh Sabzi, Flora Peyvandi, Pier Mannuccio Mannucci

Journal:

Internal and Emergency Medicine

Year:

2006

Language:

english

File:

PDF, 140 KB

english, 2006

80

Factor XI deficiency in Southern Iran: identification of a novel missense mutation

Mehran Karimi, Hamta Jafari, Saba Lahsaeizadeh, Abdolreza Afrasiabi, Ahmad Akbari, Javad Dehbozorgian, Rezvan Ardeshiri, Ilaria Guella, Rosanna Asselta, Flora Peyvandi

Journal:

Annals of Hematology

Year:

2009

Language:

english

File:

PDF, 103 KB

english, 2009

81

Perceived demands and musculoskeletal symptoms among employees of an Iranian petrochemical industry

Alireza Choobineh, Gholamreza Peyvandi Sani, Mohsen Sharif Rohani, Mohammad Gangi Pour, Masoud Neghab

Journal:

International Journal of Industrial Ergonomics

Year:

2009

Language:

english

File:

PDF, 123 KB

english, 2009

82

Variants of OCTN1–2 cation transporter genes are associated with both Crohn's disease and ulcerative colitis

O. PALMIERI, A. LATIANO, R. VALVANO, R. D'INCÀ, M. VECCHI, G. C. STURNIOLO, S. SAIBENI, F. PEYVANDI, F. BOSSA, C. ZAGARIA, A. ANDRIULLI, M. DEVOTO, V. ANNESE

Journal:

Alimentary Pharmacology & Therapeutics

Year:

2006

Language:

english

File:

PDF, 106 KB

english, 2006

83

Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease

M. Lak, F. Peyvandi, P. M. Mannucci

Journal:

British Journal of Haematology

Year:

2000

Language:

english

File:

PDF, 63 KB

english, 2000

84

von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpura

Flora Peyvandi, Silvia Ferrari, Silvia Lavoretano, Maria Teresa Canciani, Pier Mannuccio Mannucci

Journal:

British Journal of Haematology

Year:

2004

Language:

english

File:

PDF, 145 KB

english, 2004

85

The P303T mutation in the human factor VII (FVII) gene alters the conformational state of the enzyme and causes a severe functional deficiency

Flora Peyvandi, Raimondo De Cristofaro, Isabella Garagiola, Roberta Palla, Sepideh Akhavan, Raffaele Landolfi, Pier Mannuccio Mannucci

Journal:

British Journal of Haematology

Year:

2004

Language:

english

File:

PDF, 203 KB

english, 2004

86

Prospective study on the behaviour of the metalloprotease ADAMTS13 and of von Willebrand factor after bone marrow transplantation

F. Peyvandi, S. M. Siboni, D. Lambertenghi Deliliers, S. Lavoretano, N. De Fazio, B. Moroni, G. Lambertenghi Deliliers, P. Mannuccio Mannucci

Journal:

British Journal of Haematology

Year:

2006

Language:

english

File:

PDF, 129 KB

english, 2006

87

ADAMTS13 activity to antigen ratio in physiological and pathological conditions associated with an increased risk of thrombosis

Hendrik B. Feys, Maria T. Canciani, Flora Peyvandi, Hans Deckmyn, Karen Vanhoorelbeke, Pier M. Mannucci

Journal:

British Journal of Haematology

Year:

2007

Language:

english

File:

PDF, 532 KB

english, 2007

88

Different clinical severity of first episodes and recurrences of thrombotic thrombocytopenic purpura

Luca A. Lotta, Mariagabriella Mariani, Dario Consonni, Ilaria Mancini, Roberta Palla, Alberto Maino, Dragica Vucelic, Michele Pizzuti, Pier M. Mannucci, Flora Peyvandi

Journal:

British Journal of Haematology

Year:

2010

Language:

english

File:

PDF, 234 KB

english, 2010

89

Glanzmann thrombasthenia and Bernard–Soulier syndrome in south Iran

A. AFRABIASI, A. ARTONI, M. KARIMI, F. PEYVANDI, E. ASHOURI, P. M. MANNUCCI

Journal:

International Journal of Laboratory Hematology (Blackwell)

Year:

2005

Language:

english

File:

PDF, 53 KB

english, 2005

90

Comparison of attitudes towards prenatal diagnosis and termination of pregnancy for haemophilia in Iran and Italy

M. Karimi, F. Peyvandi, S. Siboni, R. Ardeshiri, A. Gringeri, P. M. Mannucci

Journal:

Year:

2004

Language:

english

File:

PDF, 41 KB

english, 2004

91

Rare bleeding disorders

F. PEYVANDI, R. J. KAUFMAN, U. SELIGSOHN, O. SALOMON, P. H. B. BOLTON-MAGGS, M. SPREAFICO, M. MENEGATTI, R. PALLA, S. SIBONI, P. M. MANNUCCI

Journal:

Year:

2006

Language:

english

File:

PDF, 119 KB

english, 2006

92

Genetic diagnosis of haemophilia and other inherited bleeding disorders

F. PEYVANDI, G. JAYANDHARAN, M. CHANDY, A. SRIVASTAVA, S. M. NAKAYA, M. J. JOHNSON, A. R. THOMPSON, A. GOODEVE, I. GARAGIOLA, S. LAVORETANO, M. MENEGATTI, R. PALLA, M. SPREAFICO, L. TAGLIABUE, R. ASSE

Journal:

Year:

2006

Language:

english

File:

PDF, 105 KB

english, 2006

93

Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India

G. JAYANDHARAN, M. SPREAFICO, A. VISWABANDYA, M. CHANDY, A. SRIVASTAVA, F. PEYVANDI

Journal:

Year:

2007

Language:

english

File:

PDF, 448 KB

english, 2007

94

Factor VIII products and inhibitor development: the SIPPET study (survey of inhibitors in plasma-product exposed toddlers)

P. M. MANNUCCI, A. GRINGERI, F. PEYVANDI, E. SANTAGOSTINO

Journal:

Year:

2007

Language:

english

File:

PDF, 63 KB

english, 2007

95

A novel mutation of α2-plasmin inhibitor gene causes an inherited deficiency and a bleeding tendency

A. MAINO, I. GARAGIOLA, A. ARTONI, S. AL-HUMOOD, F. PEYVANDI

Journal:

Year:

2008

Language:

english

File:

PDF, 81 KB

english, 2008

96

Genetic aspects and research development in haemostasis

E. G. TUDDENHAM, J. INGERSLEV, L. NORENGAARD SØRENSEN, K. CHRISTIANSEN, G. MARIANI, F. PEYVANDI, S. N. WADDINGTON, S. M. K. BUCKLEY, S. KOCHANEK, M. K. CHUAH, T. VANDENDRIESSCHE, E. BERNTORP

Journal:

Year:

2008

Language:

english

File:

PDF, 91 KB

english, 2008

97

Rare bleeding disorders

F. PEYVANDI, M. CATTANEO, A. INBAL, P. DE MOERLOOSE, M. SPREAFICO

Journal:

Year:

2008

Language:

english

File:

PDF, 89 KB

english, 2008

98

Combined FV and FVIII deficiency

M. SPREAFICO, F. PEYVANDI

Journal:

Year:

2008

Language:

english

File:

PDF, 184 KB

english, 2008

99

Gynaecological and obstetrical problems in women with different bleeding disorders

S. M. SIBONI, M. SPREAFICO, L. CALÒ, A. MAINO, E. SANTAGOSTINO, A. B. FEDERICI, F. PEYVANDI

Journal:

Year:

2009

Language:

english

File:

PDF, 217 KB

english, 2009

100

Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A

V. BAFUNNO, R. SANTACROCE, M. CHETTA, G. D’ANDREA, D. PISANELLI, F. SESSA, T. TROTTA, G. TAGARIELLO, F. PEYVANDI, M. MARGAGLIONE

Journal:

Year:

2010

Language:

english

File:

PDF, 66 KB

english, 2010

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