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DIAGNOSIS AND TREATMENT OF DISEASES ASSOCIATED WITH ABNORMALITIES OF THE COMPLEMENT SYSTEM
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Publications 2014
|
DOCUMENT |
I.F. |
CUARTILE |
|
Charignon, D.; Ghannam, A.; Defendi, F.; Ponard, D.; Monnier, N.; Trascasa, M. L.; Launay, D.; Caballero, T.; Djenouhat, K.; Fain, O.; Cichon, S.; Martin, L.; Drouet, C. Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype. ALLERGY. 2014; 69(12): 1659-1665. Artículo. |
6,028 |
D1 |
|
Blom, A. M.; Volokhina, E. B.; Fransson, V.; Stromberg, P.; Berghard, L.; Viktorelius, M.; Mollnes, T. E.; López-Trascasa, M.; van den Heuvel, L. P.; Goodship, T. H.; Marchbank, K. J.; Okroj, M. A novel method for direct measurement of complement convertases activity in human serum. CLINICAL AND EXPERIMENTAL IMMUNOLOGY. 2014; 178(1): 142-153. Artículo. |
3,037 |
Q2 |
|
Chinchilla, D. S.; Pinto, S.; Hoppe, B.; Adragna, M.; López, L.; Roldán, M. L. J.; Peña, A.; Trascasa, M. L.; Sánchez-Corral, P.; de Córdoba, S.R. Complement mutations in diacylglycerol kinase-epsilon-associated atypical hemolytic uremic syndrome. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY. 2014; 9(9): 1611-1619. Artículo. |
4,613 |
Q1 |
|
Tenorio, J.; Mansilla, A.; Valencia, M.; Martínez-Glez, V.; Romanelli, V.; Arias, P.; Castrejón, N.; Poletta, F.; Guillén-Navarro, E.; Gordo, G.; Mansilla, E.; García-Santiago, F.; González-Casado, I.; Vallespín, E.; Palomares, M.; Mori, MA.; Santos-Simarro, F.; García-Miñaur, S.; Fernández, L.; Mena, R.; Benito-Sanz, S.; del Pozo, A.; Silla, J. C.; Ibáñez, K.; López-Granados, E.; Martín-Trujillo, A.; Montaner, D.; Heath, K. E.; Campos-Barros, A.; Dopazo, J.; Nevado, J.; Monk, D.; Ruiz-Pérez, V. L.; Lapunzina, P. A new overgrowth syndrome is due to mutations in RNF125. HUMAN MUTATION. 2014; 35(12): 1436-1441. Artículo. |
5,144 |
Q1 |
|
Jozsi, M.; Reuter, S.; Nozal, P.; López-Trascasa, M.; Sánchez-Corral, P.; Prohaszka, Z.; Uzonyi, B. Autoantibodies to complement components in C3 glomerulopathy and atypical hemolytic uremic syndrome. IMMUNOLOGY LETTERS. 2014; 160(2): 163-171. Artículo. |
2,512 |
Q1 |
|
Nozal, P.; Garrido, S.; Alba-Domínguez, M.; Espinosa, L.; Peña, A.; de Córdoba, S. R.; Sánchez-Corral, P.; López-Trascasa, M. An ELISA assay with two monoclonal antibodies allows the estimation of free factor H and identifies patients with acquired deficiency of this complement regulator. MOLECULAR IMMUNOLOGY. 2014; 58: 194-200. Artículo. |
2,973 |
Q2 |
|
López-Lera, A.; Pernía, O.; López-Trascasa, M.; Cáceres, I. I. Expression of the SERPING1 gene is not regulated by promoter hypermethylation in peripheral blood mononuclear cells from patients with hereditary angioedema due to C1-inhibitor deficiency. ORPHANET JOURNAL OF RARE DISEASES. 2014; 9: 103. Artículo. |
3,358 |
Q2 |
|
Sánchez-Moreno, A.; de la Cerda, F.; Cabrera, R.; Fijo, J.; López-Trascasa, M.; Bedoya, R.; de Córdoba, S. R.; Ybot-González, P. Eculizumab in dense-deposit disease after renal transplantation. PEDIATRIC NEPHROLOGY. 2014; 29(10): 2055-2059. Artículo. |
2,856 |
Q1 |
|
Román-Ortiz, E.; Oteiza, S. M.; Pinto, S.; López-Trascasa, M.; Sánchez-Corral, P.; de Córdoba, S. R. Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid gene. PEDIATRIC NEPHROLOGY. 2014; 29(1): 149-153. Artículo. |
2.856 |
Q1 |
|
López-Lera, A.; Torres-Canizales, J. M.; Garrido, S.; Morales, A.; López-Trascasa, M. Rothmund-Thomson syndrome and glomerulonephritis in a homozygous C1q-deficient patient due to a Gly164Ser C1qC Mutation. JOURNAL OF INVESTIGATIVE DERMATOLOGY. 2014; 134(4): 1152-1154. Carta. |
7,219 |
D1 |
|
Nevado, J.; Mergener, R.; Palomares-Bralo, M.; Souza, K. R.; Vallespín, E.; Mena, R.; Martínez-Glez, V.; Mori, M. A.; Santos, F.; García-Miñaur, S.; García-Santiago, F.; Mansilla, E.; Fernández, L.; de Torres, M. L.; Riegel, M.; Lapunzina, P. New microdeletion and microduplication syndromes: a comprehensive review. GENETICS AND MOLECULAR BIOLOGY. 2014; 37(1): 210-219. Revisión. |
1,202 |
Q4 |
Publications 2009 - 2013
|
YEAR |
NAME |
I.F. |
CUARTILE |
|
2013 |
Tortajada, A.; Yébenes, H.; Abarrategui-Garrido, C.; Anter, J.; García-Fernández, J. M.; Martínez-Barricarte, R.; Alba-Domínguez, M.; Malik, T. H.; Bedoya, R.; Pérez, R. C.; Trascasa, M. L.; Pickering, M. C.; Harris, C. L.; Sánchez-Corral, P.; Llorca, O.; de Córdoba, S. R. C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation. JOURNAL OF CLINICAL INVESTIGATION. 2013; 123(6): 2434-2446. Artículo. |
13,765 |
D1 |
|
2013 |
Hebecker, M.; Alba-Domínguez, M.; Roumenina, L. T.; Reuter, S.; Hyvarinen, S.; Dragón-Durey, M. A.; Jokiranta, T. S.; Sánchez-Corral, P.; Jozsi, M. An Engineered construct combining complement regulatory and surface-recognition domains represents a minimal-size functional factor H. JOURNAL OF IMMUNOLOGY. 2013; 191(2): 912-921. Artículo. |
5,362 |
D1 |
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2013 |
Bresin, E.; Rurali, E.; Caprioli, J.; Sánchez-Corral, P.; Fremeaux-Bacchi, V.; de Córdoba, S. R.; Pinto, S.; Goodship, T. H. J.; Alberti, M.; Ribes, D.; Valoti, E.; Remuzzi, G.; Noris, M. Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY. 2013; 24(3): 475-486. Artículo. |
9,466 |
D1 |
|
2013 |
López-Lera, A.; Cabo, F. S.; Garrido, S.; Dopazo, A.; López-Trascasa, M. Disease-modifying factors in hereditary angioedema: an RNA expression-based screening. ORPHANET JOURNAL OF RARE DISEASES. 2013; 8: 77. Artículo. |
3,958 |
Q1 |
|
2013 |
Gómez-Traseira, C; López-Lera, A; Drouet, C; López-Trascasa,
M; Pérez-Fernández, E; Favier, B; Prior, N; Caballero, T. Hereditary
angioedema caused by the p.Thr309-Lys mutation in the F12 gene: A multifactorial disease. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 2013; 132(4): 986-989. Carta. |
11,248 |
D1 |
|
2012 |
Ariceta, G.; Arrizabalaga, B.; Aguirre, M.; Morteruel, E.; López-Trascasa, M. Eculizumab in the treatment of atypical hemolytic uremic syndrome in infants. AMERICAN JOURNAL OF KIDNEY DISEASES. 2012; 59(5): 707-710. Article. |
5,294 |
D1 |
|
2012 |
Leban, N.; Abarrategui-Garrido, C.; Fariza-Requejo, E.; Amiñoso-Carbonero, C.; Pinto, S.; Chibani, J. B.; Khelil, A. H.; Sánchez-Corral, P. Factor H and CFHR1 polymorphisms associated with atypical haemolytic uraemic syndrome (aHUS) are differently expressed in tunisian and in caucasian populations. INTERNATIONAL JOURNAL OF IMMUNOGENETICS. 2012; 39(2): 110-113. Article. |
1,355 |
Q4 |
|
2012 |
Kopp, A.; Strobel, S.; Tortajada, A.; de Córdoba, S. R.; Sánchez-Corral, P.; Prohaszka, Z.; López-Trascasa, M.; Jozsi, M. Atypical hemolytic uremic syndrome-associated variants and autoantibodies impair binding of factor H and factor HRelated Protein 1 to Pentraxin 3. JOURNAL OF IMMUNOLOGY. 2012; 189(4): 1858-1867. Article. |
5,52 |
Q1 |
|
2012 |
Paixao-Cavalcante, D.; López-Trascasa, M.; Skattum, L.; Giclas,
P. C.; Goodship, T. H.; de Córdoba, S. R.; Truedsson, L.; Morgan, B. P.; Harris, C. L. Sensitive and specifi c assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation. KIDNEY INTERNATIONAL. 2012; 82(10): 1084-1092. Article. |
7,916 |
D1 |
|
2012 |
Tortajada, A.; Pinto, S.; Martínez-Ara, J.; López-Trascasa, M.; Sánchez-Corral, P.; de Córdoba, S. R. Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional signifi cance. KIDNEY INTERNATIONAL. 2012; 81(1): 56-63. Article. |
7,916 |
D1 |
|
2012 |
Alba-Domínguez, M.; López-Lera, A.; Garrido, S.; Nozal, P.; González-Granado, I.; Melero, J.; Soler-Palacín, P.; Cámara, C.; López-Trascasa, M. Complement factor I defi ciency: a not so rare immune defect. Characterization of new mutations and the fi rst large gene deletion. ORPHANET JOURNAL OF RARE DISEASES. 2012; 7: 42. Article. |
4,315 |
Q1 |
|
2012 |
Marcos, C.; Lera, A. L.; Varela, S.; Linares, T.; Álvarez-Eire, M. G.; López-Trascasa, M. Clinical, biochemical, and genetic characterization of type III hereditary angioedema in 13 Northwest Spanish families. ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY. 2012; 109(3): 195-200. Article. |
3,449 |
Q1 |
|
2012 |
de la Cruz, R. M.; López-Lera, A.; López-Trascasa, M. Analysis of SERPING1 expression on hereditary angioedema patients: quantitative analysis of full-length and exon 3 splicing variants. IMMUNOLOGY LETTERS. 2012; 141(2): 158-164. Article. |
2,337 |
Q3 |
|
2012 |
Hijosa, M. M.; Melgar, A. A.; Urrutia, M. J. M.; Meseguer, C.G.; Monereo, E. J.; Torres, M. N. Living-donor transplantation after excision of unrecognized renal cancer diagnosed after transplant. PEDIATRIC NEPHROLOGY. 2012; 27(12): 2319-2321. Article. |
2,939 |
D1 |
|
2012 |
de Diego, R. P.; Lera, A. L.; Cerdán, A. F. High frequency in the delay in primary tooth loss in X-linked chronic granulomatous disease. CLINICAL IMMUNOLOGY. 2012; 145(1): 59-60. Letter. |
3,771 |
Q2 |
|
2011 |
Leban, N.; Aloui, S.; Touati, D.; Lakhdhar, R.; Skhiri, H.; Lefranc, G.; Achour, A.; Elmay, M.; LÓpez-Trascasa, M.; SÁnchez-Corral, P.; Chibani, J.; Khelil, A. H. Atypical hemolytic uremic syndrome in the Tunisian population. INTERNATIONAL UROLOGY AND NEPHROLOGY. 2011; 43(2): 559-564. Article. |
1,471 |
Q3 |
|
2011 |
Abraira, V.; Álvarez-Cermeno, J. C.; Arroyo, R.; Camara, C.; Casanova, B.; Cubillo, S.; de Andrés, C.; Espejo, C.; Fernández, O.; Ferrer, J.; Figueredo, M. A.; García-Merino, A.; García-Sánchez, M. I.; García-Trujillo, J. A.; Gómez, M.; González-Oria, C.; Gosis, A.; Izquierdo, G.; Jiménez, J.; López-Trascasa, M.; Montalban, X.; Moreno, M. J.; Muñoz, D.; Núñez, V.; Muriel, A.; Navarro, J.; Olascoaga, J.; Oreja-Guevara, C.; Prada, A.; Ramil, E.; Ramo-Tello, C.; Rodríguez, C.; Rodríguez, E.; Rodríguez-Frías, F.; Rodríguez-Antigüedad, A.; Rodríguez-Molina, J. J.; Ruiz, E.; Saiz, A.; Sarasola, E.; Simo, M.; Yague, J.; Villar, L. M. Utility of oligoclonal IgG band detection for MS diagnosis in daily clinical practice. JOURNAL OF IMMUNOLOGICAL METHODS. 2011; 371(01 feb): 170-173. Article. |
2,203 |
Q3 |
|
2011 |
Strobel, S.; Abarrategui-Garrido, C.; Fariza-Requejo, E.; Seeberger, H.; Sánchez-Corral, P.; Jozsi, M. Factor H-related protein 1 neutralizes anti-factor H autoantibodies in autoimmune hemolytic uremic syndrome. KIDNEY INTERNATIONAL. 2011; 80(4): 397-404. Article. |
6,606 |
D1 |
|
2011 |
de la Cruz, R. M.; López-Lera, A.; López-Trascasa, M. Analysis of SERPING1 expression on hereditary angioedema patients: Quantitative analysis of full-length and exon 3 splicing variants. IMMUNOLOGY
LETTERS. 2011; 141(2): 158-164. Article. |
2,526 |
Q3 |
|
2011 |
Caballero, T.; Baeza, M. L.; Cabañas, R.; Campos, A.; Cimbollek, S.; Gómez-Traseira, C.; González-Quevedo, T.; Guilarte, M.; Jurado-Palomo, J.; Larco, J. I.; López-Serrano, M. C.; López-Trascasa, M.; Marcos, C.; Muñoz-Caro, J. M.; Pedrosa, M.; Prior, N.; Rubio, M.; Sala-Cunill, A. Consensus Statement on the Diagnosis, Management, and Treatment of Angioedema Mediated by Bradykinin. Part II. Treatment, Follow-up, and Special Situations. JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY. 2011; 21(6): 422-441. Review. |
2,269 |
Q3 |
|
2011 |
Caballero, T.; Baeza, M. L.; Cabañas, R.; Campos, A.; Cimbollek, S.; Gómez-Traseira, C.; González-Quevedo, T.; Guilarte, M.; Jurado-Palomo, J.; Larco, J. I.; López-Serrano, M. C.; López-Trascasa, M.; Marcos, C.; Muñoz-Caro, J. M.; Pedrosa, M.; Prior, N.; Rubio, M.; Sala-Cunill, A. Consensus Statement on the Diagnosis, Management, and Treatment of Angioedema Mediated by Bradykinin. Part I. Classification, Epidemiology, Pathophysiology, Genetics, Clinical Symptoms, and Diagnosis. JOURNAL OF INVESTIGATIONAL
ALLERGOLOGY AND CLINICAL IMMUNOLOGY. 2011; 21(5): 333-347. Review. |
2,269 |
Q3 |
|
2011 |
Thelwell, C.; Rigsby, P.; Longstaff, C. (Lopez Trascasa, M.). An international collaborative study to establish the WHO 1st international standards for C1-inhibitor, plasma and concentrate. JOURNAL OF THROMBOSIS AND HAEMOSTASIS. 2011; 9(10): 2097-299. Editorial Material. |
5,731 |
Q1 |
|
2011 |
Lopez-Lera, A.; Garrido, S.; Roche, O.; López-Trascasa, M. SERPING1 mutations in 59 families with hereditary angioedema. MOLECULAR IMMUNOLOGY. 2011; 49(01 feb): 18-27. Article. |
2,897 |
Q2 |
|
2010 |
Fuentes, G. M. C.; Meseguer, C. G.; Carrión, A. P.; Hijosa, M. M.; García-Pose, A.; Melgar, A. A.; Torres, M. N. Long-term outcome of focal segmental glomerulosclerosis after pediatric renal transplantation. PEDIATRIC NEPHROLOGY. 2010; 25(3): 529-534. Article. |
2,183 |
Q2 |
|
2010 |
Barroso, S.; López-Trascasa, M.; Merino, D.; Álvarez, A. J.; Nuñez-Roldán, A; Sánchez, B. C7 Deficiency and Meningococcal Infection Susceptibility in Two Spanish Familias. SCANDINAVIAN JOURNAL OF IMMUNOLOGY. 2010; 72(1) 38-43. Article. |
1,935 |
Q4
|
|
2010 |
Romanelli, V.; Belinchón, A; Benito-Sanz, S.; Martínez-Glez, V.; Gracia-Bouthelier, R.; Heath, K. E.; Campos-Barros, A.; García-Minaur, S.; Fernández, L.; Meneses, H.; López-Siguero, J. P.; Guillen-Navarro, E.; Gómez-Puertas, P.; Wesselink, J. J.; Mercado, G.; Esteban-Marfil, V.; Palomo, R.; Mena, R.; Sanchez, A.; del Campo, M.; Lapunzina, P. CDKN1C (p57(Kip2)) Analysis in Beckwith-Wiedemann Syndrome (BWS) Patients: Genotype-Phenotype Correlations, Novel Mutations, and Polymorphisms. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2010; 152A (6): 1390-1397. Article. |
2,505 |
Q2
|
|
2010 |
Fuentes, G. M. C.; Román, L. E.; Hijosa, M. M.; Torres, M. N. Acute renal failure due to bilateral pieloureteral stone impaction in a 10-month-old boy. CLINICAL AND EXPERIMENTAL NEPHROLOGY. 2010; 14(4): 401-403. Article. |
1,46 |
Q3 |
|
2010 |
Álvarez-Twose, I.; de Olano, D. G.; Sánchez-Muñoz, L.; Matito, A.; Esteban-López, M. I.; Vega, A.; Mateo, M. B.; de Durana, M. D. A. D.; de la Hoz, B.; Gil, M. D. D.; Caballero, T.; Rosado, A.; Matas, I. S.; Teodosio, C.; Jara-Acevedo, M.; Mollejo, M.; García-Montero, A.; Orfao, A.; Escribano, L. Clinical, biological, and molecular characteristics of clonal mast cell disorders presenting with systemic mast cell activation symptoms. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 2010; 125(6): 1269-1278. Article. |
9,273 |
Q1 |
|
2010 |
Piñana, E.; Lei, S. H.; Merino, R.; Melgosa, M.; De La Vega, R.; Gonzáles-Obeso, E.; Ramírez, E.; Borobia, A.; Carcas, A. DRESS-syndrome on sulfasalazine and naproxen treatment for juvenile idiopathic arthritis and reactivation of human herpevirus 6 in an 11-year-old caucasian boy. JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS. 2010; 35(3): 365-370. Article. |
1,649 |
Q3
|
|
2010 |
Martínez-Barricarte, R.; Heurich, M.; Valdés-Canedo, F.; Vázquez-Martul, E.; Torreira, E.; Montes, T.; Tortajada, A.; Pinto, S.; López-Trascasa, M.; Morgan, B. P.; Llorca, O.; Harris, C. L.; de Cordoba, S. R. Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation. JOURNAL OF CLINICAL INVESTIGATION. 2010; 120(10): 3702-3712. Article. |
14,152 |
Q1
|
|
2010 |
Jurado-Palomo, J.; Cabanas, R.; Prior, N.; Bobolea, I. D.; Fiandor-Román, A. M.; López-Serrano, M. C.; Quirce, S.; Bellón, T. Use of the Lymphocyte Transformation Test in the Diagnosis of DRESS Syndrome Induced by Ceftriaxone and Piperacillin-tazobactam: Two Case Reports. JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY. 2010; 20(5): 433-436. Article. |
1,489 |
Q3
|
|
2010 |
Sánchez-Corral, P.; Melgosa, M. Advances in understanding the aetiology of atypical Haemolytic Uraemic Síndrome. BRITISH JOURNAL OF HAEMATOLOGY. 2010; 150(5): 529-542. Review. |
4,942 |
Q1 |
|
2010 |
López-Lera, A.; Favier, B.; de la Cruz, R. M.; Garrido, S.; Drouet, C.; López-Trascasa, M. A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation. JOURNAL OF ALLERGY AND CLINICAL. 2010; 126(6): 1307-1310. Letter. |
9,273 |
Q1
|
|
2009 |
Cruzado, JM; de Cordoba, SR; Melilli, E; Bestard, O; Rama, I; Sanchez-Corral, P; Lopez-Trascasa, M; Navarro, I; Torras, J; Goma, M; Grinyo, JM. Successful Renal Transplantation in a Patient with Atypical Hemolytic Uremic Syndrome Carrying Mutations in Both Factor I and MCP. AMERICAN JOURNAL OF TRANSPLANTATION. 2009; 9(6): 1477-1483 |
6,433 |
Q1
|
|
2009 |
Vaudry, W; Ettenger, R; Jara, P; Varela-Fascinetto, G; Bouw, MR; Ives, J; Walker, R. Valganciclovir Dosing According to Body Surface Area and Renal Function in Pediatric Solid Organ Transplant Recipients. AMERICAN JOURNAL OF TRANSPLANTATION. 2009; 9(3): 636-643 |
6,433 |
Q1
|
|
2009 |
Rubio Rodríquez F., Melgosa Hijosa M. Hipertensión arterial en la infancia. ANALES DE PEDIATRIA CONTINUADA. 2009; 7: 270-278 |
N/A |
N/A
|
|
2009 |
Pedrosa, M; Caballero, T; Gomez-Traseira, C; Olveira, A; Lopez-Serrano, C. Usefulness of abdominal ultrasonography in the follow-up of patients with hereditary C1-inhibitor deficiency. ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY. 2009; 102(6): 483-486 |
2,457 |
Q2
|
|
2009 |
Jurado-Palomo, J; Caballero, T; Fernandez-Nieto, M; Quirce, S. OCCUPATIONAL ASTHMA CAUSED BY ARTIFICIAL CYANOACRYLATE FINGERNAILS. ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY. 2009; 102(5): 440-441 |
2,457 |
Q2
|
|
2009 |
Valdivieso, R; Cevallos, F; Caballero, MT; Quirce, S. Chronic urticaria caused by folic acid. ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY. 2009; 103(1): 81-82 |
2,457 |
Q2
|
|
2009 |
Abarrategui-Garrido, C; Martinez-Barricarte, R; Lopez-Trascasa, M; de Cordoba, SR; Sanchez-Corral, P. Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome. BLOOD. 2009; 114(19): 4261-4271 |
10,555 |
Q1
|
|
2009 |
Garcia, BE; Gamboa, PM; Asturias, JA; Lopez-Hoyos, M; Sanz, ML. Guidelines on the Clinical Usefulness of Determination of Specific Immunoglobulin E to Foods. JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY. 2009; 19(6): 423-432 |
1,189 |
Q3
|
|
2009 |
Saland, JM; Ruggenenti, P; Remuzzi, G. Liver-Kidney Transplantation to Cure Atypical Hemolytic Uremic Syndrome. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY. 2009; 20(5): 940-949 |
7,689 |
Q1
|
|
2009 |
Lopez-Trascasa, M; Gil-Aguado, A; Capozzi, A; Sorice, M. Association of anti-C1 inhibitor and anti-protein S antibodies in a patient with primary antiphospholipid syndrome. LUPUS. 2009; 18(2): 182-183 |
2,586 |
Q3
|
|
2009 |
Lopez-Lera, A; Garrido, S; de la Cruz, RM; Fontan, G; Lopez-Trascasa, M. Molecular characterization of three new mutations causing C5 deficiency in two non-related families. MOLECULAR IMMUNOLOGY. 2009; 46: 2340-2347 |
3,202 |
Q3
|
|
|
|
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