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In vitro secretion of matrix metalloprotease 9 is a prognostic marker in childhood acute lymphoblastic leukemia

Leukemia research, 2010-01, Vol.34 (1), p.24-31

2010

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Proteomic profile of pre - B2 lymphoblasts from children with acute lymphoblastic leukemia

Clinical proteomics, 2014-08, Vol.11

2014

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Proteomic profile of pre - B2 lymphoblasts from children with acute lymphoblastic leukemia (ALL) in relation with the translocation (12; 21)

Clinical proteomics, 2014-01, Vol.11 (1), p.31-31, Article 31

2014

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Optimization of an animal model of experimental autoimmune encephalomyelitis achieved with a multiple MOG35-55 peptide in C57BL6/J strain of mice

Journal of autoimmunity, 2003, Vol.20 (1), p.51-61

2003

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Optimization of an animal model of experimental autoimmune encephalomyelitis achieved with a multiple MOG(35-55)peptide in C57BL6/J strain of mice

Journal of autoimmunity, 2003-02, Vol.20 (1), p.51-61

2003

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Optimization of an animal model of experimental autoimmune encephalomyelitis achieved with a multiple MOG 35–55peptide in C57BL6/J strain of mice

Journal of autoimmunity, 2003, Vol.20 (1), p.51-61

2003

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Protéomique et auto-anticorps

M.S. Médecine sciences, 2005-08, Vol.21 (8-9), p.759-764

2005

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Proteomics and autoantibody

M.S. Médecine sciences, 2005-08, Vol.21 (8-9), p.759-764

2005

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Immune Neuroendocrine Interactions: Implications for Reproductive Physiologya

Annals of the New York Academy of Sciences, 1989-07, Vol.564 (1), p.261-266

1989

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Immune Neuroendocrine Interactions: Implications for Reproductive Physiology

Annals of the New York Academy of Sciences, 1989, Vol.564 (1), p.261-266

1989

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Toward a neurocircuit-based taxonomy to guide treatment of obsessive-compulsive disorder

Molecular psychiatry, 2021-09, Vol.26 (9), p.4583-4604

2021

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Obsessive-compulsive disorder

Nature reviews. Disease primers, 2019-08, Vol.5 (1), p.52-52, Article 52

2019

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Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders

Blood reviews, 2013-07, Vol.27 (4), p.167-178

2013

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A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndrome

Annals of neurology, 2017-07, Vol.82 (1), p.133-138

2017

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Clinical Significance of Quantifying Pneumocystis jirovecii DNA by Using Real-Time PCR in Bronchoalveolar Lavage Fluid from Immunocompromised Patients

Journal of Clinical Microbiology, 2012-02, Vol.50 (2), p.227-231

2012

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Expanding the heuristic neurocircuit-based taxonomy to guide treatment for OCD: reply to the commentary "Probing the genetic and molecular correlates of connectome alterations in obsessive-compulsive disorder"

Molecular psychiatry, 2022-09, Vol.27 (9), p.3560-3561

2022

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Critical review on biofilm methods

Critical reviews in microbiology, 2017-05, Vol.43 (3), p.313-351

2017

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Neurocircuit models of obsessive-compulsive disorder: limitations and future directions for research

Revista brasileira de psiquiatria, 2022-03

2022

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Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer

Blood cells, molecules, & diseases, 2016-01, Vol.56 (1), p.9-22

2016

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El territorio como recurso: Movilidad y apropiación del espacio en México y Centroamérica

2018

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Spontaneous radial nerve palsy with hourglass-like constriction

BMJ case reports, 2023-08, Vol.16 (8)

2023

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A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia

American journal of human genetics, 2010-11, Vol.87 (5), p.721-727

2010

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Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1

Blood cells, molecules, & diseases, 2023-11, Vol.103, p.102780-102780, Article 102780

2023

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Azole Preexposure Affects the Aspergillus fumigatus Population in Patients

Antimicrobial Agents and Chemotherapy, 2012-09, Vol.56 (9), p.4948-4950

2012

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In vitro secretion of matrix metalloprotease 9 is a prognostic marker in childhood acute lymphoblastic leukemia

Proteomic profile of pre - B2 lymphoblasts from children with acute lymphoblastic leukemia

Proteomic profile of pre - B2 lymphoblasts from children with acute lymphoblastic leukemia (ALL) in relation with the translocation (12; 21)

Optimization of an animal model of experimental autoimmune encephalomyelitis achieved with a multiple MOG35-55 peptide in C57BL6/J strain of mice

Optimization of an animal model of experimental autoimmune encephalomyelitis achieved with a multiple MOG(35-55)peptide in C57BL6/J strain of mice

Optimization of an animal model of experimental autoimmune encephalomyelitis achieved with a multiple MOG 35–55peptide in C57BL6/J strain of mice

Protéomique et auto-anticorps

Proteomics and autoantibody

Immune Neuroendocrine Interactions: Implications for Reproductive Physiologya

Immune Neuroendocrine Interactions: Implications for Reproductive Physiology

Toward a neurocircuit-based taxonomy to guide treatment of obsessive-compulsive disorder

Obsessive-compulsive disorder

Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders

A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndrome

Clinical Significance of Quantifying Pneumocystis jirovecii DNA by Using Real-Time PCR in Bronchoalveolar Lavage Fluid from Immunocompromised Patients

Expanding the heuristic neurocircuit-based taxonomy to guide treatment for OCD: reply to the commentary "Probing the genetic and molecular correlates of connectome alterations in obsessive-compulsive disorder"

Critical review on biofilm methods

Neurocircuit models of obsessive-compulsive disorder: limitations and future directions for research

Measurement Fidelity of Clinical Assessment Methods in a Global Study on Identifying Reproducible Brain Signatures of Obsessive-Compulsive Disorder

Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer

El territorio como recurso: Movilidad y apropiación del espacio en México y Centroamérica

Spontaneous radial nerve palsy with hourglass-like constriction

A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia

Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1

Azole Preexposure Affects the Aspergillus fumigatus Population in Patients

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