A case of intracranial hemorrhage in a neonate with congenital factor VII deficiency by Won Seok Lee, Young Sil Park

Subjects: “…Congenital factor VII deficiency…”
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Spontaneous subgaleal haemorrhage in a newborn: A rare presentation of congenital factor VII deficiency due to homogenous missense mutation of factor VII gene by Ajoy Kumar Garg, Siva Chaitanya, S.K. Patnaik, Vivek Kumar

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Hemophagocytic lymphohistiocytosis and congenital factor VII deficiency: a case report by Xiong Wang, Ning Tang, Wei Chang, Yanjun Lu, Dengju Li

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Genotype and phenotype correlation in intracranial hemorrhage in neonatal factor VII deficiency among Thai children by Traivaree C, Monsereenusorn C, Meekaewkunchorn A, Laoyookhong P, Suwansingh S, Boonyawat B

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Factor VII Deficiency in Systemic Mastocytosis with an Associated Myeloid Neoplasm by Giorgio Rosati, Sofia Camerlo, Alessandro Fornari, Valerio Marci, Barbara Montaruli, Alessandro Morotti

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Acquired factor VII deficiency causing severe bleeding disorder secondary to AL amyloidosis of the liver by Anthony L. Nguyen, Muhammad Kamal, Ravi Raghavan, Gayathri Nagaraj

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Factor VII deficiency-related recurrent hemarthrosis in a female child – When to suspect? by Siyaram Didel, Abhishek H. L. Purohit, Deepthi Krishna, Varuna Vyas, Kuldeep Singh

Subjects: “…factor vii deficiency…”
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Dental extraction in congenital factor Vll deficiency with inhibitor – a case report by Nayar Geeta, Pillai Vijayakumar Narayana, Mathew Sheena, Menon Gokul Das

Subjects: “…congenital factor vii deficiency with inhibitor…”
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Late diagnosed factor VII deficiency – a rare but significant haemorrhagic diathesis by Karolina Małgorzata Różycka, Beata Kuczyńska, Kinga Podsiadło, Małgorzata Mitura-Lesiuk, Irena Woźnica- Karczmarz

Subjects: “…factor vii deficiency…”
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Asymptomatic intracranial hemorrhage in a newborn with congenital factor VII deficiency and successful treatment with recombinant activated factor VII by Zeynep İnce, Özgül Bulut, Melike Tuğrul-Aksakal, Ayşegül Ünüvar, Ömer Devecioğlu, Asuman Çoban

Subjects: “…factor VII deficiency…”
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Fiona’s FVII footprint by Mulders Greta, Tuinhout Mirjam

Subjects: “…factor vii deficiency…”
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AryoSeven RT (Coagulation factor VIIa, recombinant) safety and efficacy study among congenial factor VII deficient patients in Iraq by Nidal Karim Al-Rahal, Ahmed Shemran Alwataify, Safa Mohammed Shawkat, Israa Almusawi, Azeezah Mohammed Mohsin

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A case-report of the unprovoked thrombotic event in a patient with thymoma and severe FVII deficiency by Lei Li, Xi Wu, Wenman Wu, Qiulan Ding, Xuefeng Wang

Subjects: “…Factor VII deficiency…”
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The effect of the chemical chaperone 4-phenylbutyrate on secretion and activity of the p.Q160R missense variant of coagulation factor FVII by Elisabeth Andersen, Maria Eugenia Chollet, Marcello Baroni, Mirko Pinotti, Francesco Bernardi, Ellen Skarpen, Per Morten Sandset, Grethe Skretting

Subjects: “…Factor VII deficiency…”
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Case report of recurrent bleeding in an infant with isolated prolonged prothrombin time due to congenital factor VII deficiency---a riddle solved by Mimi Ganguly, Saurabh Sutradhar, Arghya Rajbangshi, Amrita Pattnaik, Dipshikha Maiti

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Synonymous variant at the terminal nucleotide in exon 3 of F7 causes abnormal splicing: A case report by Liya Wang, Wenshan Zeng, Yeqing Qian, Yixi Sun, Min Chen, Bei Liu, Junjie Hu, Ping Yu, Minyue Dong

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The Factor VII Variant p.A354V-p.P464Hfs: Clinical versus Intracellular and Biochemical Phenotypes Induced by Chemical Chaperones by Elisabeth Andersen, Maria Eugenia Chollet, Francesco Bernardi, Alessio Branchini, Marcello Baroni, Guglielmo Mariani, Alberto Dolce, Angelika Batorova, Ellen Skarpen, Christiane Filion Myklebust, Grethe Skretting, Per Morten Sandset

Subjects: “…factor VII deficiency…”
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Phenotypic and genotypic analysis of patients with congenital factor VII deficiency in a multicenter study in Thailand by Ampaiwan Chuansumrit, Surapan Parapakpenjune, Rungrote Natesirinilkul, Patcharee Komvilaisak, Werasak Sasanakul, Nongnuch Sirachainan, Anchalee Aramthienthamrong, Chorthip Wattanasutthipong, Kittima Kanchanakumhan, Kunrada Inthawong, Montana Chantaraniyom, Naonpan Pongpaothai, Nattaporntira Phalakornkul, Nisakorn Khumchan, Pacharapan Surapolchai, Panjarat Sowittayasakul, Somporn Wangruangsathit

Subjects: “…Congenital factor VII deficiency…”
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Case of concurrent factor VII and factor XI deficiencies manifesting as spontaneous lower extremity compartment syndrome by Joseph P. Marshalek, David Yashar, Karen Huynh, Sarah Tomassetti

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