A patient with AL amyloidosis and severe factor X deficiency has been in complete haematological remission with normal factor X activity for 7 years following high-dose chemotherapy. A case study and literature review

scientific article published in January 2010

A patient with AL amyloidosis and severe factor X deficiency has been in complete haematological remission with normal factor X activity for 7 years following high-dose chemotherapy. A case study and literature review is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P698PubMed publication ID20184115

P2093author name stringMayer J
Adam Z
Hájek R
Krejcí M
Pour L
Chlupová G
Kissová J
Matýková M
Penka M
Simonides J
Slechtová M
Stavarová Y
P433issue1
P407language of work or nameCzechQ9056
P921main subjectfactor X deficiencyQ18555036
coagulation factor x humanQ28859740
AL amyloidosisQ4652470
P304page(s)67-78
P577publication date2010-01-01
P1433published inVnitřní lékařstvíQ27713817
P1476titleA patient with AL amyloidosis and severe factor X deficiency has been in complete haematological remission with normal factor X activity for 7 years following high-dose chemotherapy. A case study and literature review
P478volume56

Reverse relations

Q35085505Acquired factor X deficiency in light chain amyloidosis: a report of 2 Korean casescites workP2860

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