Hepatic familial amyloidosis caused by a new mutation in the apolipoprotein AI gene: clinical and pathological features

scientific article published on 01 June 2001

Hepatic familial amyloidosis caused by a new mutation in the apolipoprotein AI gene: clinical and pathological features is …

instance of (P31):

scholarly article

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P356	DOI	10.1111/J.1572-0241.2001.03887.X
P698	PubMed publication ID	11419842

P2093	author name string	Rodés J
		Campistol JM
		Bruguera M
		Caballería J
		Solé M
P2860	cites work	Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures	Q26778382
		Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis.	Q34334873
		Human lysozyme gene mutations cause hereditary systemic amyloidosis	Q34362632
		Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene	Q38337830
		The systemic amyloidoses	Q41596634
		Improvement in the polyneuropathy associated with familial amyloid polyneuropathy after liver transplantation	Q47629217
		Liver transplantation as a treatment for familial amyloidotic polyneuropathy	Q72647122
P433	issue	6
P304	page(s)	1872-1876
P577	publication date	2001-06-01
P1433	published in	The American Journal of Gastroenterology	Q7713501
P1476	title	Hepatic familial amyloidosis caused by a new mutation in the apolipoprotein AI gene: clinical and pathological features
P478	volume	96

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cites work (P2860)

Q61445851	A new genetic variant of hereditary apolipoprotein A-I amyloidosis: a case-report followed by discussion of diagnostic challenges and therapeutic options
Q31029305	Amyloidogenicity and clinical phenotype associated with five novel mutations in apolipoprotein A-I.
Q37164492	Hereditary apolipoprotein AI-associated amyloidosis in surgical pathology specimens: identification of three novel mutations in the APOA1 gene

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