Visualitzant R - Articles científics per títol

New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II

Musri, Melina Mara; Venturi, Veronica; Ferrer, Xènia; Romero Cortadellas, Lídia; Hernandez Viedma, Gonzalo; Leoz Allegretti, María del Pilar; Beneitez Pastor, David; Ortuño Cabrero, Ana (MDPI, 2023-06-09)

New genes involved in Angelman syndrome-like: Expanding the genetic spectrum

Aguilera, Cinthia; Gabau, Elisabeth; Ramirez-Mallafre, Ariadna; Brun-Gasca, Carme; Dominguez-Carral, Jana; Delgadillo, Veronica; Padilla Sirera, Natalia; De la Cruz Montserrat, Fco. Xavier (Public Library of Science, 2021-10-15)

New insights into pneumonia in patients on prolonged mechanical ventilation: need for a new paradigm addressing dysbiosis

Rello Condomines, Jordi; Schrenzel, Jacques; Tejo, Alexandre M. (Sociedade Brasileira de Pneumologia e Tisiologia, 2021-06-23)

New methods for the diagnosis and monitoring of cognitive function in patients with type 2 diabetes

Simó Canonge, Rafael; Ciudin Mihai, Andreea (Frontiers Media, 2022-12-01)

Next-Generation Sequencing for Confronting Virus Pandemics

Quer Sivila, Josep; Colomer Castell, Sergi; Campos Martinez, Carolina; Andrés Verges, Cristina; Piñana Moro, Maria; González Sánchez, Alejandra; Garcia Cehic, Damir; Pumarola Suñé, Tomàs; Rodríguez Frias, Francisco; Antón Pagarolas, Andres; Tabernero Caellas, David; Ibañez Lligoña, Marta; Cortese, Maria Francesca (MDPI, 2022-03-14)

Next-generation Sequencing in Bone Marrow Failure Syndromes and Isolated Cytopenias: Experience of the Spanish Network on Bone Marrow Failure Syndromes

Galvez, Eva; Vallespin, Elena; Arias-Salgado, Elena G.; Sánchez-Valdepeñas, Carmen; Giménez, Yari; Navarro, Susana; Díaz de Heredia Rubio, Maria Cristina (Lippincott, Williams & Wilkins, 2021-03-09)

NFκB and NLRP3/NLRC4 inflammasomes regulate differentiation, activation and functional properties of monocytes in response to distinct SARS-CoV-2 proteins

Tsukalov, Ilya; Sánchez Cerrillo, Ildefonso; Rajas, Olga; Ávalos Perez-Urria , Elena; Iturricastillo, Gorane; Esparcia, Laura; Buzon, Maria Jose; Genescà Ferrer, Meritxell (Nature Portfolio, 2024-03-07)

Nine controversial questions about augmentation therapy for alpha-1 antitrypsin deficiency: a viewpoint

Anzueto, Antonio R.; Miravitlles, Marc; Barrecheguren, Miriam (European Respiratory Society, 2023-12-31)

Non-Alcoholic Fatty Liver Disease in Patients with Polycystic Ovary Syndrome: A Systematic Review, Meta-Analysis, and Meta-Regression

Manzano Nuñez, Ramiro; Santana-Dominguez, Marta; Rivera Esteban, Jesus Manuel; Sabiote Cartes, Clara; de Sena Fernández, Elena; Bañares Sanchez, Juan; Tacke, Frank; Pericàs Pulido, Juan Manuel (MDPI, 2023-01-20)

Non-Invasive Tests of Liver Fibrosis Help in Predicting the Development of Hepatocellular Carcinoma among Patients with NAFLD

Pons Delgado, Mònica; Rivera Esteban, Jesus Manuel; Manzano Nuñez, Ramiro; Bañares Sanchez, Juan; Bermúdez Ramos, María; Salcedo Allende, Maria Teresa; Castells Fusté, Lluis; Minguez Rosique, Beatriz; Pericàs Pulido, Juan Manuel; Vargas Blasco, Victor Manuel; Augustin Recio, Salvador (MDPI, 2022-05)

Non-prosthetic implant-related femur fractures in post-polio patients

Castellanos Alonso, Sara; Tomás Hernández, Jordi; Teixidor Serra, Jordi; Selga Marsa, Jordi; Piedra Calle, Carlos Alberto; Andrés Peiró, José Vicente (Elsevier, 2023-08)

Noninvasive detection of microsatellite instability in patients with endometrial cancer

Casas-Arozamena, Carlos; Moiola, Cristian Pablo; Vilar, Ana; Bouso, Marta; Cueva, J.; Cabrera Diaz, Silvia; García Jiménez, Angel; Gil Moreno, Antonio; Colas Ortega, Eva (Wiley, 2023-05-15)

Noninvasive predictors of clinically significant portal hypertension in NASH cirrhosis: Validation of ANTICIPATE models and development of a lab-based model

Rabiee, Anahita; Deng, Yanhong; Ciarleglio, Maria; Chan, Jean L.; Pons Delgado, Mònica; Genescà Ferrer, Joan; Garcia-Tsao, Guadalupe (Wiley, 2022-12)

Novel Dent disease 1 cellular models reveal biological processes underlying ClC-5 loss-of-function

Durán Fernández, Mónica; Cantero Recasens, Gerard; Butnaru, Cristian M.; Malhotra, Vivek; Sarro Tauler, Eduard; Meseguer Navarro, Anna; Ariceta Iraola, Gema; Burballa Tàrrega, Carla (Oxford University Press, 2021-08-01)

Novel genes and sex differences in COVID-19 severity

Cruz, Raquel; Diz de Almeida, Silvia; Lopez de Heredia, M; Quintela, Ines; Pita, Guillermo; Palom Agusti, Adriana; Buti Ferret, Maria; Ceballos, Francisco (Oxford University Press, 2022-11-11)

Novel Splicing Mutation in MTM1 Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy

Bosco, Luca; Leone, Daniela; Costa Comellas, Laura; Monforte, Mauro; Pane, Marika; Mercuri, Eugenio (MDPI, 2022-09-07)

Novel strategies in nephrology: what to expect from the future?

Copur, Sidar; Tanriover, Cem; Yavuz, Furkan; Soler Romeo, Maria Jose; Covic, Adrian; Kanbay, Mehmet; Ortiz Arduan, Alberto (Oxford University Press, 2023-02)

Novel variant in HHAT as a cause of different sex development with partial gonadal dysgenesis associated with microcephaly, eye defects, and distal phalangeal hypoplasia of both thumbs: Case report

Baz Redón, Noelia; Soler Colomer, Laura; Fernández Cancio, Mónica; Benito-Sanz, Sara; Garrido-Pontnou, Marta; Moline Marimon, Teresa; Clemente Leon, Maria; Camats Tarruella, Nuria; Yeste Fernandez, Diego (Frontiers Media, 2022-10-11)

NR4A3: A Key Nuclear Receptor in Vascular Biology, Cardiovascular Remodeling, and Beyond

Rodríguez Sinovas, Antonio; Corrales Insa, Irene; Alonso Nieto, Judith; Ballester-Servera, Carme; Cañes Esteve, Laia; Rodriguez, Cristina; Martínez-González, José (MDPI, 2021-10-21)

Nuclear and cytosolic pS727-STAT3 levels correlate with overall survival of patients affected by clear cell renal cell carcinoma (ccRCC)

Arevalo Bautista, Jazmine Paola; Lorente García, David; Trilla Herrera, Enric; Salcedo Allende, Maria Teresa; Morote Robles, Joan; Meseguer Navarro, Anna (Nature Research, 2021-03-26)

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Visualitzant VHIR - Articles científics per títol

New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II

New genes involved in Angelman syndrome-like: Expanding the genetic spectrum

New insights into pneumonia in patients on prolonged mechanical ventilation: need for a new paradigm addressing dysbiosis

New methods for the diagnosis and monitoring of cognitive function in patients with type 2 diabetes

Next-Generation Sequencing for Confronting Virus Pandemics

Next-generation Sequencing in Bone Marrow Failure Syndromes and Isolated Cytopenias: Experience of the Spanish Network on Bone Marrow Failure Syndromes

NFκB and NLRP3/NLRC4 inflammasomes regulate differentiation, activation and functional properties of monocytes in response to distinct SARS-CoV-2 proteins

Nine controversial questions about augmentation therapy for alpha-1 antitrypsin deficiency: a viewpoint

Non-Alcoholic Fatty Liver Disease in Patients with Polycystic Ovary Syndrome: A Systematic Review, Meta-Analysis, and Meta-Regression

Non-Invasive Tests of Liver Fibrosis Help in Predicting the Development of Hepatocellular Carcinoma among Patients with NAFLD

Non-prosthetic implant-related femur fractures in post-polio patients

Noninvasive detection of microsatellite instability in patients with endometrial cancer

Noninvasive predictors of clinically significant portal hypertension in NASH cirrhosis: Validation of ANTICIPATE models and development of a lab-based model

Novel Dent disease 1 cellular models reveal biological processes underlying ClC-5 loss-of-function

Novel genes and sex differences in COVID-19 severity

Novel Splicing Mutation in MTM1 Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy

Novel strategies in nephrology: what to expect from the future?

Novel variant in HHAT as a cause of different sex development with partial gonadal dysgenesis associated with microcephaly, eye defects, and distal phalangeal hypoplasia of both thumbs: Case report

NR4A3: A Key Nuclear Receptor in Vascular Biology, Cardiovascular Remodeling, and Beyond

Nuclear and cytosolic pS727-STAT3 levels correlate with overall survival of patients affected by clear cell renal cell carcinoma (ccRCC)

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Visualitzant VHIR - Articles científics per títol

New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II ﻿

New genes involved in Angelman syndrome-like: Expanding the genetic spectrum ﻿

New insights into pneumonia in patients on prolonged mechanical ventilation: need for a new paradigm addressing dysbiosis ﻿

New methods for the diagnosis and monitoring of cognitive function in patients with type 2 diabetes ﻿

Next-Generation Sequencing for Confronting Virus Pandemics ﻿

Next-generation Sequencing in Bone Marrow Failure Syndromes and Isolated Cytopenias: Experience of the Spanish Network on Bone Marrow Failure Syndromes ﻿

NFκB and NLRP3/NLRC4 inflammasomes regulate differentiation, activation and functional properties of monocytes in response to distinct SARS-CoV-2 proteins ﻿

Nine controversial questions about augmentation therapy for alpha-1 antitrypsin deficiency: a viewpoint ﻿

Non-Alcoholic Fatty Liver Disease in Patients with Polycystic Ovary Syndrome: A Systematic Review, Meta-Analysis, and Meta-Regression ﻿

Non-Invasive Tests of Liver Fibrosis Help in Predicting the Development of Hepatocellular Carcinoma among Patients with NAFLD ﻿

Non-prosthetic implant-related femur fractures in post-polio patients ﻿

Noninvasive detection of microsatellite instability in patients with endometrial cancer ﻿

Noninvasive predictors of clinically significant portal hypertension in NASH cirrhosis: Validation of ANTICIPATE models and development of a lab-based model ﻿

Novel Dent disease 1 cellular models reveal biological processes underlying ClC-5 loss-of-function ﻿

Novel genes and sex differences in COVID-19 severity ﻿

Novel Splicing Mutation in MTM1 Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy ﻿

Novel strategies in nephrology: what to expect from the future? ﻿

Novel variant in HHAT as a cause of different sex development with partial gonadal dysgenesis associated with microcephaly, eye defects, and distal phalangeal hypoplasia of both thumbs: Case report ﻿

NR4A3: A Key Nuclear Receptor in Vascular Biology, Cardiovascular Remodeling, and Beyond ﻿

Nuclear and cytosolic pS727-STAT3 levels correlate with overall survival of patients affected by clear cell renal cell carcinoma (ccRCC) ﻿

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Guies i ajudes

Directe a...

Coneix Scientia

Guies i ajudes

Directe a...

New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II

New genes involved in Angelman syndrome-like: Expanding the genetic spectrum

New insights into pneumonia in patients on prolonged mechanical ventilation: need for a new paradigm addressing dysbiosis

New methods for the diagnosis and monitoring of cognitive function in patients with type 2 diabetes

Next-Generation Sequencing for Confronting Virus Pandemics

Next-generation Sequencing in Bone Marrow Failure Syndromes and Isolated Cytopenias: Experience of the Spanish Network on Bone Marrow Failure Syndromes

NFκB and NLRP3/NLRC4 inflammasomes regulate differentiation, activation and functional properties of monocytes in response to distinct SARS-CoV-2 proteins

Nine controversial questions about augmentation therapy for alpha-1 antitrypsin deficiency: a viewpoint

Non-Alcoholic Fatty Liver Disease in Patients with Polycystic Ovary Syndrome: A Systematic Review, Meta-Analysis, and Meta-Regression

Non-Invasive Tests of Liver Fibrosis Help in Predicting the Development of Hepatocellular Carcinoma among Patients with NAFLD

Non-prosthetic implant-related femur fractures in post-polio patients

Noninvasive detection of microsatellite instability in patients with endometrial cancer

Noninvasive predictors of clinically significant portal hypertension in NASH cirrhosis: Validation of ANTICIPATE models and development of a lab-based model

Novel Dent disease 1 cellular models reveal biological processes underlying ClC-5 loss-of-function

Novel genes and sex differences in COVID-19 severity

Novel Splicing Mutation in MTM1 Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy

Novel strategies in nephrology: what to expect from the future?

Novel variant in HHAT as a cause of different sex development with partial gonadal dysgenesis associated with microcephaly, eye defects, and distal phalangeal hypoplasia of both thumbs: Case report

NR4A3: A Key Nuclear Receptor in Vascular Biology, Cardiovascular Remodeling, and Beyond

Nuclear and cytosolic pS727-STAT3 levels correlate with overall survival of patients affected by clear cell renal cell carcinoma (ccRCC)