Results
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881.
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PTX3, A prototypical long pentraxin, is an early indicator of acute myocardial infarction in humans. [electronic resource] by
- Peri, G
- Introna, M
- Corradi, D
- Iacuitti, G
- Signorini, S
- Avanzini, F
- Pizzetti, F
- Maggioni, A P
- Moccetti, T
- Metra, M
- Cas, L D
- Ghezzi, P
- Sipe, J D
- Re, G
- Olivetti, G
- Mantovani, A
- Latini, R
Producer: 20000831
In:
Circulation vol. 102
Availability: No items available.
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882.
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883.
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884.
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885.
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886.
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887.
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Plasma pentraxin 3 levels are associated with carotid IMT in type 1 diabetic patients. [electronic resource] by
- Katakami, Naoto
- Kaneto, Hideaki
- Sakamoto, Fumie
- Takahara, Mitsuyoshi
- Irie, Yoko
- Fujisawa, Keiko
- Miyashita, Kazuyuki
- Yasuda, Tetsuyuki
- Matsuoka, Taka-aki
- Yoshiuchi, Kazutomi
- Sakamoto, Ken'ya
- Kuroda, Akio
- Matsuhisa, Munehide
- Kosugi, Keisuke
- Shimomura, Iichiro
Producer: 20130923
In:
Diabetes research and clinical practice vol. 99
Availability: No items available.
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888.
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889.
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890.
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Genetic PTX3 deficiency and aspergillosis in stem-cell transplantation. [electronic resource] by
- Cunha, Cristina
- Aversa, Franco
- Lacerda, João F
- Busca, Alessandro
- Kurzai, Oliver
- Grube, Matthias
- Löffler, Jürgen
- Maertens, Johan A
- Bell, Alain S
- Inforzato, Antonio
- Barbati, Elisa
- Almeida, Bruno
- Santos e Sousa, Pedro
- Barbui, Anna
- Potenza, Leonardo
- Caira, Morena
- Rodrigues, Fernando
- Salvatori, Giovanni
- Pagano, Livio
- Luppi, Mario
- Mantovani, Alberto
- Velardi, Andrea
- Romani, Luigina
- Carvalho, Agostinho
Producer: 20140211
In:
The New England journal of medicine vol. 370
Availability: No items available.
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891.
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Diagnostic sensitivity of abdominal fat aspiration in cardiac amyloidosis. [electronic resource] by
- Quarta, Candida Cristina
- Gonzalez-Lopez, Esther
- Gilbertson, Janet A
- Botcher, Nichola
- Rowczenio, Dorota
- Petrie, Aviva
- Rezk, Tamer
- Youngstein, Taryn
- Mahmood, Shameem
- Sachchithanantham, Sajitha
- Lachmann, Helen J
- Fontana, Marianna
- Whelan, Carol J
- Wechalekar, Ashutosh D
- Hawkins, Philip N
- Gillmore, Julian D
Producer: 20180613
In:
European heart journal vol. 38
Availability: No items available.
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892.
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893.
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894.
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895.
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896.
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897.
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Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene. [electronic resource] by
- Booth, D R
- Tan, S Y
- Booth, S E
- Tennent, G A
- Hutchinson, W L
- Hsuan, J J
- Totty, N F
- Truong, O
- Soutar, A K
- Hawkins, P N
- Bruguera, M
- Caballería, J
- Solé, M
- Campistol, J M
- Pepys, M B
Producer: 19960812
In:
The Journal of clinical investigation vol. 97
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898.
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Labial salivary gland biopsy is a reliable test for the diagnosis of primary and secondary amyloidosis. A prospective clinical and immunohistologic study in 59 patients. [electronic resource] by
- Hachulla, E
- Janin, A
- Flipo, R M
- Saïle, R
- Facon, T
- Bataille, D
- Vanhille, P
- Hatron, P Y
- Devulder, B
- Duquesnoy, B
Producer: 19930604
In:
Arthritis and rheumatism vol. 36
Availability: No items available.
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899.
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900.
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In vivo supramolecular templating enhances the activity of multivalent ligands: a potential therapeutic against the Escherichia coli O157 AB5 toxins. [electronic resource] by
- Kitov, Pavel I
- Mulvey, George L
- Griener, Thomas P
- Lipinski, Tomasz
- Solomon, Dmitry
- Paszkiewicz, Eugenia
- Jacobson, Jared M
- Sadowska, Joanna M
- Suzuki, Missao
- Yamamura, Ken-Ichi
- Armstrong, Glen D
- Bundle, David R
Producer: 20081222
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 105
Availability: No items available.
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