Search Results - "Jesús Pozo‐Román" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Response to growth hormone in patients with RNPC3 mutations

Response to growth hormone in patients with RNPC3 mutations

by Martos‐Moreno, Gabriel Á, Travieso‐Suárez, Lourdes, Pozo‐Román, Jesús, Muñoz‐Calvo, María T, Chowen, Julie A, Frilander, Mikko J, Pérez‐Jurado, Luis A, Hawkins, Federico G, Argente, Jesús
Published in EMBO molecular medicine (07.09.2020)

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Letter: reassuringly normal response to ACTH in children treated with swallowed topical corticosteroids for eosinophilic oesophagitis

Letter: reassuringly normal response to ACTH in children treated with swallowed topical corticosteroids for eosinophilic oesophagitis

by Rodríguez Manchón, Silvia, Domínguez Ortega, Gloria, Bacelo Ruano, Irene, Martínez Ibeas, María Angeles, Pozo Román, Jesús, Cañedo Villarroya, Elvira, Muñoz Codoceo, Rosa Ana
Published in Alimentary pharmacology & therapeutics (01.06.2019)

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Response to growth hormone in patients with RNPC3 mutations

Response to growth hormone in patients with RNPC3 mutations

by Martos‐Moreno, Gabriel Á, Travieso‐Suárez, Lourdes, Pozo‐Román, Jesús, Muñoz‐Calvo, María T, Chowen, Julie A, Frilander, Mikko J, Pérez‐Jurado, Luis A, Hawkins, Federico G, Argente, Jesús
Published in EMBO molecular medicine (01.07.2018)

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Brachydactyly type C due to a nonsense mutation in the GDF5 gene

Brachydactyly type C due to a nonsense mutation in the GDF5 gene

by Travieso-Suárez, Lourdes, Pereda, Arrate, Pozo-Román, Jesús, Pérez de Nanclares, Guiomar, Argente, Jesús
Published in Anales de Pediatría (01.02.2018)

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Journal Article

Response to growth hormone in patients with RNPC 3 mutations

Response to growth hormone in patients with RNPC 3 mutations

by Martos‐Moreno, Gabriel Á, Travieso‐Suárez, Lourdes, Pozo‐Román, Jesús, Muñoz‐Calvo, María T, Chowen, Julie A, Frilander, Mikko J, Pérez‐Jurado, Luis A, Hawkins, Federico G, Argente, Jesús
Published in EMBO molecular medicine (07.09.2020)

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Journal Article

Thickening of the pituitary stalk in children and adolescents with central diabetes insipidus: Causes and consequences

Thickening of the pituitary stalk in children and adolescents with central diabetes insipidus: Causes and consequences

by Corredor Andrés, Beatriz, Muñoz Calvo, María Teresa, López Pino, Miguel Ángel, Márquez Rivera, María, Travieso Suárez, Lourdes, Pozo Román, Jesús, Argente, Jesús
Published in Anales de Pediatría (01.05.2019)

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Journal Article

Response to growth hormone in patients with RNPC 3 mutations

Response to growth hormone in patients with RNPC 3 mutations

by Gabriel Á Martos‐Moreno, Lourdes Travieso‐Suárez, Jesús Pozo‐Román, María T Muñoz‐Calvo, Chowen, Julie A, Frilander, Mikko J, Luis A Pérez‐Jurado, Hawkins, Federico G, Argente, Jesús
Published in EMBO molecular medicine (01.07.2018)

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Journal Article

Acquired partial lipodystrophy (Barraquer–Simons syndrome) and IgA nephropathy

Acquired partial lipodystrophy (Barraquer–Simons syndrome) and IgA nephropathy

by de Lucas-Collantes, Carmen, Pozo-Román, Jesús, Aparicio-López, Cristina, de Prada-Vicente, Inmaculada, Argente, Jesús
Published in Nefrología (01.09.2016)

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Engrosamiento del tallo hipofisario en niños y adolescentes con diabetes insípida central: causas y consecuencias

Engrosamiento del tallo hipofisario en niños y adolescentes con diabetes insípida central: causas y consecuencias

by Corredor Andrés, Beatriz, Muñoz Calvo, María Teresa, López Pino, Miguel Ángel, Márquez Rivera, María, Travieso Suárez, Lourdes, Pozo Román, Jesús, Argente, Jesús
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.05.2019)

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Mutation in RET gene: Prophylactic thyroidectomy and postoperative follow-up

Mutation in RET gene: Prophylactic thyroidectomy and postoperative follow-up

by Villamayor Martín, Raquel, Bartucci, Andrea, Muñoz Calvo, María Teresa, Pozo Román, Jesús, Argente, Jesús
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.11.2016)

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Braquidactilia tipo C debida a mutación de parada en el gen GDF5

Braquidactilia tipo C debida a mutación de parada en el gen GDF5

by Travieso-Suárez, Lourdes, Pereda, Arrate, Pozo-Román, Jesús, Pérez de Nanclares, Guiomar, Argente, Jesús
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.02.2018)

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Lipodistrofia parcial adquirida (síndrome de Barraquer-Simons) y nefropatía IgA

Lipodistrofia parcial adquirida (síndrome de Barraquer-Simons) y nefropatía IgA

by de Lucas-Collantes, Carmen, Pozo-Román, Jesús, Aparicio-López, Cristina, de Prada-Vicente, Inmaculada, Argente, Jesús
Published in Nefrología (01.09.2016)

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Endocrine Sequelae in 157 Pediatric Survivors of Hematopoietic Stem Cell Transplantation (HSCT)

Endocrine Sequelae in 157 Pediatric Survivors of Hematopoietic Stem Cell Transplantation (HSCT)

by Güemes, María, Martín-Rivada, Álvaro, Bascuas Arribas, Marta, Andrés-Esteban, Eva María, Molina Angulo, Blanca, Pozo Román, Jesús, Argente, Jesús
Published in Journal of the Endocrine Society (15.12.2022)

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Erratum To: Response to growth hormone in patients with RNPC3 mutations

Erratum To: Response to growth hormone in patients with RNPC3 mutations

by Martos‐Moreno, Gabriel Á, Travieso‐Suárez, Lourdes, Pozo‐Román, Jesús, Muñoz‐Calvo, María T, Chowen, Julie A, Frilander, Mikko J, Pérez‐Jurado, Luis A, Hawkins, Federico G, Argente, Jesús
Published in EMBO molecular medicine (07.09.2020)

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Journal Article

Brachydactyly type C due to a nonsense mutation in the GDF5 gene

Brachydactyly type C due to a nonsense mutation in the GDF5 gene

by Travieso-Suárez, Lourdes, Pereda, Arrate, Pozo-Román, Jesús, Pérez de Nanclares, Guiomar, Argente, Jesús
Published in Anales de Pediatría (01.02.2018)

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Journal Article

Thickening of the pituitary stalk in children and adolescents with central diabetes insipidus: Causes and consequences

Thickening of the pituitary stalk in children and adolescents with central diabetes insipidus: Causes and consequences

by Corredor Andrés, Beatriz, Muñoz Calvo, María Teresa, López Pino, Miguel Ángel, Márquez Rivera, María, Travieso Suárez, Lourdes, Pozo Román, Jesús, Argente, Jesús
Published in Anales de Pediatría (01.05.2019)

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Journal Article

LZTR1: Genotype Expansion in Noonan Syndrome

LZTR1: Genotype Expansion in Noonan Syndrome

by Güemes, María, Martín-Rivada, Álvaro, Ortiz-Cabrera, Neimar Valentina, Martos-Moreno, Gabriel Ángel, Pozo-Román, Jesús, Argente, Jesús
Published in Hormone research in paediatrics (01.03.2020)

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Primary Dwarfism, Microcephaly, and Chorioretinopathy due to a PLK4 Mutation in Two Siblings

Primary Dwarfism, Microcephaly, and Chorioretinopathy due to a PLK4 Mutation in Two Siblings

by Martín-Rivada, Álvaro, Pozo-Román, Jesús, Güemes, María, Ortiz-Cabrera, Nelmar Valentina, Pérez-Jurado, Luis A, Argente, Jesús
Published in Hormone research in paediatrics (01.04.2021)

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Journal Article

Mutation in RET gene: Prophylactic thyroidectomy and postoperative follow-up

Mutation in RET gene: Prophylactic thyroidectomy and postoperative follow-up

by Villamayor Martín, Raquel, Bartucci, Andrea, Muñoz Calvo, María Teresa, Pozo Román, Jesús, Argente, Jesús
Published in Anales de Pediatría (01.11.2016)

Get full text

Journal Article

Acquired partial lipodystrophy (Barraquer-Simons syndrome) and IgA nephropathy

Acquired partial lipodystrophy (Barraquer-Simons syndrome) and IgA nephropathy

by de Lucas-Collantes, Carmen, Pozo-Román, Jesús, Aparicio-López, Cristina, de Prada-Vicente, Inmaculada, Argente, Jesús
Published in Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia (01.09.2016)

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Journal Article