Добавил:
Sekretar
kiopkiopkiop18@yandex.ru
t.me/Prokururor I Вовсе не секретарь, но почту проверяю
Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз:
Предмет:
Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_3099_Библиотеки_им_академика_М_И_Перельмана.pdf
Bibliography
117
precursor cells / John Quinn and Kwee L. Yong -- The genetic and
epigenetic mechanisms underlying the behaviour of myeloma / Martin F.
Kaiser, Kevin D. Boyd, and Gareth J. Morgan -- The myeloma bone
marrow environment and survival signaling / Kwee L. Yong, John Quinn,
and Asim Khwaja -- Immune dysfunction in multiple myeloma / Guy Pratt
and Paul Moss -- Myeloma bone disease: pathogenesis of bone destruction
and therapeutic strategies / Andrew Chantry and Neil Rabin -- Principles
of pathway directed therapy for myeloma / Yu-Tzu Tai and Kenneth C.
Anderson -- Monoclonal gammopathy of undetermined significance
(MGUS) and smoldering multiple myeloma / Efstathios Kastritis and
Meletios A. Dimopoulos -- Multiple myeloma: management of de novo
disease / T. Guglielmelli, P. Sonneveld, A. Broyl, and Antonio Palumbo --
Treatment of relapsed/refractory myeloma / Matthew J. Streetly, Jacob
Laubach, Paul Richardson, and Stephen A. Schey -- Solitary bone and
extramedullary plasmacytoma / Shirley Sa -- Amyloidosis / Ashutosh D.
Wechalekar, Simon W. Dubrey, and Raymond L. Comenzo --
Waldenstrom's macroglobinemia/ lymphoplasmocytic lymphoma / Steven
P. Treon and Giampaolo Merlini -- Castleman's disease / Karthik
Ramasamy -- Poems syndrome and paraproteinaemic syndromes:
management and follow-up / Angela Dispenzieri and Suzanne R. Hayman
-- Treatment of emergent peripheral neuropathy and plasma cell disorders
/ Charise Gleason, Melanie Watson, and Sagar Lonial -- Management of
renal failure in multiple myeloma / Aneel Paulus, Pooja Advani, Nabeel
Aslam, and Asher Alban Chanan-Khan -- The management of infection in
myeloma / Christopher P. Conlon. Subjects: Multiple Myeloma. Notes:
Includes bibliographical references and index.
Neoplastic diseases of the blood / [edited by] Peter H. Wiernik ... [et al.].
LCCN: 2012944838 Edition: 5th ed. Published/Created: New York:
Springer, c2013. Description: xix, 1431 p.: ill. (chiefly col.), ports.; 28 cm.
ISBN: 9781461437635 (hbk.: alk. paper) 1461437636 (hbk.: alk. paper)
9781461437642 (ebook) 1461437644 (ebook) LC classification: RC643
.N46 2013 Related names: Wiernik, Peter H. Contents: A history of the
chronic leukemias / John M. Goldman and Myrtle Y. Gordon -- Etiology
and epidemiology of chronic myeloid leukemia / Maren Rohrbacher and
Joerg Hasford -- Pathology of the chronic myeloid leukemias / Barbara J.
Bain -- Molecular biology and cytogenetics of chronic myeloid leukemia /
Alfonso Quints Cardama, Hagop Kantarjian, and Jorge Cortes --
Diagnosis and treatment of chronic myeloid leukemia / Stephen G.
Raquel Watts
118
O'Brien and John M. Goldman -- Etiology and epidemiology of CLL /
Dalemari Crowther-Swanepoel, Daniel Catovsky, and Richard S.
Houlston -- Histopathology, morphology, and immunophenotyping of
CLL / Abraham M. Varghese ... [et al.] -- Molecular biology and
cytogenetics of chronic lymphocytic leukemia / David Oscier, Anne
Gardiner, and Jonathan C. Strefford -- Treatment of chronic lymphocytic
leukemia and related disorders / Gautam Borthakur and Susan O'Brien --
Hairy cell leukemia / Sejal A. Jhatakia, Darren S. Sigal, and Alan Saven --
The pathogenesis, diagnosis, and treatment of polycythaemia vera / Mark
A. Dawson and Brian J.P. Huntly -- Diagnosis and treatment of essential
thrombocythemia and primary myelofibrosis / John T. Reilly -- History of
acute leukemia / Emil J. Freireich -- The etiology of acute leukemia /
Jessica N. Nichol, Sarit Assouline, and Wilson H. Miller -- Epidemiology
and hereditary aspects of acute leukemia / Martha S. Linet ... [et al.] --
Classification of the acute leukemias: cytochemical and morphologic
considerations / Nukhet N. Tuzuner and John M. Bennett --
Immunobiology of acute leukemia / Elisabeth Paietta -- Cytogenetics of
acute leukemia / Nyla A. Heerema and Susana Catalina Raimondi --
Diagnosis and treatment of childhood acute lymphoblastic leukemia /
Dario Campana and Ching-Hon Pui -- Diagnosis and treatment of adult
acute lymphoblastic leukemia / Nicola Goekbuget and Dieter Hoelzer --
Diagnosis and treatment of childhood acute myeloid leukemia / David A.
Sweetser and Howard J. Weinstein -- Diagnosis and treatment of adult
acute myeloid leukemia other than acute promyelocytic leukemia / Peter
H. Wiernik -- Acute promyelocytic leukemia / Peter H. Wiernik, Robert E.
Gallagher, and Martin S. Tallman -- Therapy-related acute myelogenous
leukemia / Gabriela Bernadeta Iwanski ... [et al.] -- The myelodysplastic
syndromes / Kenneth Miller and Igor Rozenvald -- History of multiple
myeloma / David P. Steensma and Robert A. Kyle -- Cytokines and signal
transduction in multiple myeloma / Dharminer Chauhan and Kenneth C.
Anderson -- Epidemiology of multiple myeloma / Dalsu Baris ... [et al.] --
Immunoglobulins and laboratory recognition of monoclonal proteins /
Jerry Katzmann ... [et al.] -- Cytogenetic abnormalities in MGUS and
myeloma / Rafael Fonseca, P. Leif Bergsagel, and W. Michael Kuehl --
Molecular genetics of myeloma / Brian Van Ness -- Prognosis and staging
of multiple myeloma / Jess F. San-Miguel, Ramn Garca-Sanz, and
Norma C. Gutirrez -- Diagnosis and treatment of multiple myeloma / S.
Vincent Rajkumar and Robert A. Kyle -- Complications and special
presentations of plasma cell myeloma / Joan Blad
e and Laura Rosiol --
Bibliography
119
Waldenström's macroglobulinemia / Efstathios Kastritis and Meletios A.
Dimopoulos -- Heavy-chain disease / Dietlind L. Wahner-Roedler and
Robert A. Kyle -- Diagnosis and therapy of immunoglobulin light chain
amyloidosis (AL amyloidosis) / Morie A. Gertz and Robert A. Kyle --
Monoclonal gammopathy of undetermined significance / Robert A. Kyle
and S. Vincent Rajkumar -- Historical landmarks in the understanding of
the lymphomas / Marshall A. Lichtman -- Genetics in lymphomagenesis /
Sigurdur Y. Kristinsson ... [et al.] -- Epidemiology and hereditary aspects
of Hodgkin and non-Hodgkin lymphomas / Seymour Grufferman --
Pathology of non-Hodgkin's and Hodgkin's lymphomas / L. Jeffrey
Medeiros -- Immunology of the lymphomas / Carla Kurkjian and Howard
Ozer -- Cytogenetics of lymphomas / Meaghan Wall and Lynda J.
Campbell -- Diagnosis and treatment of Hodgkin's lymphoma / Peter H.
Wiernik, Monica Balzarotti, and Armando Santoro -- Radiotherapeutic
management of lymphomas / John P. Plastaras ... [et al.] -- Diagnosis and
treatment of non-Hodgkin's lymphoma of adults / Edward A. Faber, Jr. ...
[et al.] -- Non-Hodgkin lymphoma of childhood / Tony H. Truong, Sheila
Weitzman, and Robert J. Arceci -- Lymphoma in other diseases / William
B. Ershler, Barbara K. Dunn, and Dan L. Longo -- Supportive care for
patients with leukemia: a historical perspective / Charles A. Schiffer --
Prevention of infections in patients with hematological malignancies /
Marcio Nucci ... [et al.] -- Evaluation and management of bacterial and
fungal infections occurring in patients with a hematological malignancy: a
2011 update / James C. Wade -- Viral infections in patients with
hematological malignancies / Jack W. Hsu ... [et al.] -- Therapuetic
cytapheresis, plasmapheresis, and plasma exchange in neoplastic diseases
of the blood / Janice P. Dutcher -- Red cell transfusions in patients with
hematologic malignancies / Karen E. King and Paul M. Ness -- Platelet
and granulocyte transfusion / Janice P. Dutcher -- Alternative sources of
hematopoietic stem cells and their clinical applications / Jonathan A.
Gutman, Shelly Heimfeld, and H. Joachim Deeg -- HLA typing in support
of hematopoietic cell transplantation from unrelated donors / Effie W.
Petersdorf ... [et al.] -- Special care of blood and marrow stem transplant
patients / Hillard M. Lazarus, Lisa M. Arfons, and Richard J. Creger --
Hematopoietic growth factors in the supportive care and treatment of
patients with hematologic neoplasms / Belinda R. Avalos and Edward A.
Copelan -- Bleeding and thrombosis in hematologic neoplasia /
Aleksandra Ciszewski and Thomas DeLoughery -- Psychological aspects
of hematological neoplasms / Tomer T. Levin. Subjects: Blood--Diseases.
Raquel Watts
120
Hematological oncology. Hematologic Neoplasms. Leukemia.
Lymphoma. Multiple Myeloma. Notes: Previous ed.: Cambridge:
Cambridge University Press, 2003. Includes bibliographical references
and index.
New-opathies: an emerging molecular reclassification of human disease /
[edited by] Errol C. Friedberg ... [et al.]. LCCN: 2012008086
Published/Created: New Jersey: World Scientific, c2012. Description:
xvii, 291 p.; 24 cm. ISBN: 9789814355681 (hardcover: alk. paper)
9814355682 (hardcover: alk. paper) LC classification: RB151 .N48 2012
Related names: Friedberg, Errol C. Contents: Laminopathies / William T.
Dauer and Howard J. Worman -- Inflammasomopathies: diseases linked to
the NLRP3 inflammasome / Dominic De Nardo ... [et al.] -- Amyloidosis /
Morie A. Gertz -- Adiposopathy / Harold E. Bays and J. Michael
Gonzalez-Campoy -- Telomeropathies / Rodrigo T. Calado and Neal S.
Young -- FANC-BLM-opathies: recent progress in the understanding of
molecular pathogenesis of fanconi anemia and its connection with bloom
syndrome / Toshiyasu Taniguchi ... [et al.] -- Lysosomopathies:
pathophysiology and treatment of lysosomal storage diseases / Beth L.
Thurberg -- Phosphatopathies / Makoto Kuro-o. Subjects: Disease--
genetics. Disease--classification. Genetic Heterogeneity. Notes: Includes
bibliographical references and index.
Non-fibrillar amyloidogenic protein assemblies: common cytotoxins
underlying degenerative diseases / Farid Rahimi, Gal Bitan, editors.
LCCN: 2011944432 Published/Created: Dordrecht; New York: Springer,
c2012. Description: viii, 565 p.: ill.; 25 cm. ISBN: 9789400727731 (alk.
paper) 9400727739 (alk. paper) 9789400727748 (e-ISBN) 9400727747
(e-ISBN) LC classification: RC632.A5 N66 2012 Related names: Rahimi,
Farid. Bitan, Gal. Subjects: Amyloidosis. Amyloidogenic Proteins--
toxicity. Cytotoxins--adverse effects. Neuro-degenerative Diseases --
etiology. Notes: Includes bibliographical references and index.
Peripheral nerve disorders / volume editors, Grard Said and Christian
Krarup. LCCN: 2014397727 Uniform title: Peripheral nerve disorders
(Said) Published/Produced: Edinburgh: Elsevier, 2013. Description: xx,
987 pages: illustrations (some color); 27 cm. ISBN: 9780444529022
(cloth) 0444529020 (cloth) LC classification: RC409 .P455 2013 RC332
.H3 v.115 2013 Related names: Said, G. (Gerard), editor. Krarup,
Christian, editor. Summary: "Disorders of the peripheral nervous system
Bibliography
121
(PNS) are the cause of prominent neurological symptoms including
weakness, sensory loss, pain and autonomic dysfunction associated with
deficits, morbidity and mortality. These disorders may be primary
hereditary or cryptogenic neurologic disorders confined to the PNS or part
of the pathology of both the central nervous system and the PNS. Most
PNS disorders are secondary to other system disorders and may be
responsive to treatment of the primary disease. Important advances have
been obtained in several areas including molecular genetics, biochemistry,
immunology, morphology and physiology that have enhanced our
understanding of the causes and consequences of damage to peripheral
nerve. Understanding of both these groups of PNS diseases has greatly
expanded over recent years and has led to important advances of treatment
both to protect and to repair damages of peripheral nerve. This volume
provides an overview of the state-of-the-art of examination, diagnosis and
treatment of these very diverse disorders and will be of interest to both the
research and clinical neuroscience and neurology communities"--
Publisher's description. Contents: Prelude to the peripheral neuropathies --
Microscopic anatomy: normal structure -- Gross anatomy and
development of the peripheral nervous system -- Physiology and
pathophysiology of myelinated nerve fibers -- Biology of Schwann cells --
Neurophysiological approach to disorders of peripheral nerve -- Testing
the autonomic nervous system -- Imaging of the peripheral nervous system
-- The nerve biopsy: indications, technical aspects, and contribution -- The
cutaneous nerve biopsy: technical aspects, indications, and contribution --
Antibody testing in peripheral nerve disorders -- DNA testing in
hereditary neuropathies -- Examination and clinical care of the patient
with neuropathy -- How to explore a patient with a chronic axonal
polyneuropathy -- Evaluation of a patient with suspected chronic
demyelinating polyneuropathy -- Sensory-motor assessment in clinical
research trials -- Management of painful neuropathies -- Diagnosis of
brachial and lumbosacral plexus lesions -- Compression and entrapment
neuropathies -- Facial nerve palsy and hemifacial spasm -- The Guillain-
Barr syndrome -- Chronic inflammatory demyelinative polyneuropathy --
Treatment of chronic inflammatory demyelinating polyradiculoneuropathy
-- Multifocal motor neuropathy -- Neuropathy and monoclonal
gammopathy -- Vasculitic neuropathy -- Sarcoidosis of the peripheral
nervous system -- Leprous neuropathy -- HIV peripheral neuropathy --
Human T-cell leukemia virus (HTLV)-associated neuropathy -- Herpes
virus infection in the peripheral nervous system -- Lyme neuroborreliosis -
Raquel Watts
122
- Diabetic neuropathy -- Biology of diabetic neuropathy -- Uremic
neuropathy -- Porphyric neuropathy -- Fabry disease -- Transthyretin
familial amyloid polyneuropathy -- Hereditary gelsolin amyloidosis --
Malignant cell infiltration in the peripheral nervous system --
Paraneoplastic neuropathy -- Drug-induced neuropathies -- Late radiation
injury to peripheral nerves -- Neuromuscular complications of critical
illness -- The surgery of peripheral nerves (including tumors) -- Peripheral
neuropathy in the elderly -- Dominant Charcot-Marie-Tooth syndrome and
cognate disorders -- Recessively transmitted predominantly motor
neuropathies -- Early onset (childhood) monogenic neuropathies --
Hereditary sensory and autonomic neuropathies -- Peripheral nerve
involvement in hereditary cerebellar and multisystem degenerative
disorders -- Giant axonal neuropathy -- Neurofibromatosis type 1 (NF1):
diagnosis and management -- Neurofibromatosis type 2 (NF2): diagnosis
and management. Subjects: Nerves, Peripheral--Diseases. Peripheral
Nervous System Diseases. Notes: Includes bibliographic references and
index. Additional formats: Online version: Said, G. (Gerard). Peripheral
Nerve Disorders. Elsevier, 2013 9780444633552 (OCoLC)857277776
Series: Handbook of clinical neurology; volume 115, 3rd series Handbook
of clinical neurology; 3rd ser., v. 115.
Protein aggregation and fibrillogenesis in cerebral and systemic amyloid
disease / J. Robin Harris, editor. LCCN: 2012953928 Published/Produced:
Dordrecht; New York: Springer, 2012. Description: xvii, 648 pages:
illustrations (some color); 24 cm. ISBN: 9789400754157 (alk. paper)
9400754159 (alk. paper) LC classification: QP552.A45 P76 2012 Related
names: Harris, James R., editor. Contents: Introduction and technical
survey: Protein aggregation and fibrillogenesis -- Fibril formation by short
synthetic peptides -- In vitrooligomerization and fibrillogenesis of
amyloid-beta peptides -- Tau fibrillogenesis -- Prion protein aggregation
and fibrillogenesisin vitro -- Alpha-synuclein aggregation and modulating
factors -- Pathological self-aggregation of [beta](2)-microglobulin: A
challenge for protein biophysics -- Islet amyloid polypeptide: Aggregation
and fibrillogenesisin vitroand its inhibition -- Mechanisms of transthyretin
aggregation and toxicity -- Fibrillogenesis of huntingtin and other
glutamine containing proteins -- Aggregation and fibrillogenesis of
proteins not associated with disease: a few case studies -- Experimental
inhibition of peptide fibrillogenesis by synthetic peptides, carbohydrates
and drugs -- Experimental inhibition of fibrillogenesis and neurotoxicity
Bibliography
123
by amyloid-beta (abeta) and other disease-related peptides/proteins by
plant extracts and herbal compounds -- Alzheimer's disease -- Modeling
the polyglutamine aggregation pathway in Huntington's disease: from
basic studies to clinical applications -- Parkinson's disease -- Human prion
diseases: From kuru to variant Creutzfeldt-jakob disease -- Animal prion
diseases -- [beta](2)-Microglobulin amyloidosis -- Systemic AA
amyloidosis -- Familial amyloidotic polyneuropathy and transthyretin --
The challenge of systemic immunoglobulin light-chain amyloidosis (AL).
Subjects: Amyloid beta-protein. Aggregation (Chemistry) Amyloidosis.
Proteins. Amyloidosis--physiopathology. Amyloid. Cell Aggregation.
Plague, Amyloid. Protein Folding. Aggregation (Chemistry) Amyloid
beta-protein. Amyloidosis. Proteins. Subject keywords: Medicine. Notes:
Includes bibliographical references and index. Series: Subcellular
biochemistry, 0306-0225; 65 Sub-cellular biochemistry; v. 65. 0306-0225
Samuels and Ropper's neurological CPCs from the New England Journal of
Medicine / Martin Allen Samuels, Allan H. Ropper. LCCN: 2012020639
Personal name: Samuels, Martin A. Published/Created: New York: Oxford
University Press, c2013. Description: xviii, 331 p.: ill.; 24 cm. ISBN:
9780199927517 (pbk.: alk. paper) LC classification: RC348 .S26 2013
Variant title: Neurological CPCs from the New England Journal of
Medicine Related titles: New England journal of medicine. Related
names: Ropper, Allan H. Contents: A 51 year old man with neck pain
(foramen magnum meningioma): CPC 19-1979 -- A 68 year old man with
a gait disorder (Paget disease with extramedullary hematopoiesis): CPC
23-1981 -- A 16 year old boy with confusion (parainfectious
encephalopathy from mycoplasma): CPC 35-1981 -- A 63 year old woman
with agitation and an extrapyramidal syndrome (multisystem atrophy):
CPC 23-1983 -- A 29 year old woman with myalgia and muscle weakness
(porphyria): CPC 39-1984 -- A 62 year old man with progressive
polyneuropathy (amyloidosis): CPC 26-1986 -- A 26 year old woman with
dilated cardiomyopathy and a stroke (pheochromocytoma): CPC 15-1988
-- A 35 year old man with changed mental status and multiple
intracerebral lesions (neurosyphilis): CPC 32-1991 -- A 71 year old man
with a rash, muscle weakness and respiratory failure (paraproteinemic
neuropathy): CPC 21-1993 -- A 49 year old man with an intracranial mass
(primary central nervous system lymphoma): CPC 36-1994 -- An 18 year
old man with headache, ataxia, and slurred speech (Q fever cellulitis):
CPC 38-1996 -- A 43 year old woman with adult respiratory distress
Raquel Watts
124
syndrome (Rocky Mountain spotted fever): CPC 32-1997 -- A 74 year old
woman with diarrhea and fever followed by multiple cranial nerve palsies
(Campylobacter related Guillain-Barre syndrome): CPC 39-1999 -- A 31
year old man with an apparent seizure and a cerebral lesion
(schistosomiasis): CPC 21-2001 -- A 61 year old man with headache and
multiple infarcts (Trousseau syndrome): CPC 31-2002 -- A 77 year old
man with ear pain, difficulty speaking and altered mental status (otic
bacterial meningitis): CPC 34-2007 -- A 49 year old man with peripheral
neuropathy and ascites (POEMS syndrome): CPC 7-2010 -- A 54 year old
woman with dizziness and falls (pheochromocytoma): CPC 14-2010.
Subjects: Nervous System Diseases--diagnosis--Case Reports. Nervous
System Diseases--diagnosis--Collected Works. Nervous System Diseases-
-pathology--Case Reports. Nervous System Diseases--pathology--
Collected Works. Neurologic Manifestations--Case Reports. Neurologic
Manifestations--Collected Works. Notes: Includes bibliographical
references and index.
RELATED NOVA PUBLICATIONS
COGNITIVE DECLINE IN MCI AND AD: Β -AMYLOIDOSIS
AND TAUOPATHY VERSUS CEREBROVASCULAR RISK
*
Cheryl J. Aine, PhD
1,†
, Janice E. Knoefel, MD
2
,
John C. Adair, MD
3
, Lori Sanfratello, PhD
1
and Julia M. Stephen, PhD
2
1
Department of Radiology, University of New Mexico
School of Medicine, Albuquerque, New Mexico, US
2
Department of Internal Medicine, Geriatrics, University of
New Mexico School of Medicine, Albuquerque, New Mexico, US
3
Department of Neurology, University of New Mexico
School of Medicine, Albuquerque, New Mexico, US
4
The Mind Research Network, Albuquerque, New Mexico, US
Although much effort is underway to understand the pathological
processes leading to mild cognitive impairment (MCI) and Alzheimer’s
*
The full version of this chapter can be found in Mild Cognitive Impairment (MCI): Symptoms,
Causes, Risk Factors and Clinical Outcomes, edited by Leon R. Kline and Tim A. Crosby,
published by Nova Science Publishers, Inc, New York, 2013.
†
Corresponding author: Cheryl J. Aine PhD, Department of Radiology, MSC10 5530, 1
University of New Mexico, Albuquerque, NM 87131-0001. Phone: +1 505 272-5557; Fax:
+1 505 272-8002; E-mail: aine@unm.edu.
Related Nova Publications
126
disease (AD) in the quest for a cure, to date little progress has been made in
developing viable treatments for AD. Recent studies attempting toto determine
the initiating event of AD (β-amyloid plaques vs. neurofibrillary tangles) may
be interesting from a scientific perspective, but they do not seem to aid in
finding a cure. Perhaps more effort should be expended on effects of chronic
cerebrovascular diseases in elderly, such as hypertension and
hypercholesterolemia, which have been shown to result in premature cognitive
decline. Unfortunately, there are no studies that have determined the optimal
levels of blood pressure and lipids for cognition across the lifespan. Another
issue concerns the opinion expressed by some investigators that only
“validated” imaging techniques should be used for documenting
neurodegeneration in MCI and AD. Does this stifle progress toward finding
novel methodologies for documenting neurodegeneration in preclinical AD?
These issues are explored herein.
AMYLOIDOSIS: ETIOLOGY,
PATHOGENESIS AND DIAGNOSIS
*
Laura Díez
1
, Antonio G. Prado
2
and Isabel G. Guijarro
3
Department of Otolaryngology, El Bierzo Hospital
1
,
POVISA
2
, CHOU
3
, Spain
Amyloidoses are a heterogeneous group of diseases characterized by the
deposition of fibrillar protein in extracellular tissue space. Amyloid deposits
consist of a stable, insoluble aggregate of precursor proteins that have adopted
an antiparallel beta pleated sheet configuration, having an amorphous and
eosinophilic appearance. Although the reason for the accumulation of fibrils is
poorly understood, several factors may be involved seeing as there are certain
characteristics in precursor molecules that make them amyloidogenic, thus
predisposing them to amyloid fibril formation. Different types of amyloidosis
exist depending on the fibrillar protein precursor. The most common are: AL,
which is associated with plasma cell dyscrasia; AA, associated with chronic
*
The full version of this chapter can be found in Amyloids: Composition, Functions and
Pathology, edited by Irene P. Halcheck and Nancy R. Vernon, published by Nova Science
Publishers, Inc, New York, 2012.