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European Journal of Medical Genetics
|
March 22, 2021
Description of four patients with TRIP11 variants expand the clinical spectrum of odontochondroplasia (ODCD) and demonstrate the existence of common variants
Mariana Del Pino, Maria José Sanchez-Soler, Manuel Parrón-Pajares, et al.
Archivos De Bronconeumologia
|
September 5, 2006
[High-resolution computed tomography patterns of organizing pneumonia]
Alberto Bravo Soberón, María Isabel Torres Sánchez, Francisco García Río, et al.
American Journal of Medical Genetics. Part A
|
August 29, 2020
Spondyloepiphyseal dysplasia type Stanescu: Expanding the clinical and molecular spectrum of a very rare type II collagenopathy
André M Travessa, Francisca Díaz-González, Teresa Mirco, et al.
Pediatric Transplantation
|
November 3, 2025
Effect of Muscle Mass on Catch-Up Growth After Liver Transplant in Infants With Biliary Atresia
María D Lledín, Manuel Parrón-Pajares, David Andrade-Guerrero, et al.
European Journal of Medical Genetics
|
August 18, 2021
Early clinical and radiological improvement in a young boy with metaphyseal anadysplasia type 2
Samuel Bonilla-Fornés, Lourdes Galán-Ledesma, Pilar Méndez Pérez, et al.
The Pediatric Infectious Disease Journal
|
July 5, 2023
Acute Suppurative Thyroiditis in Children: Clinical Decision-Making
Silvia Gómez, Cristina Mora, Dorleta López de Suso, et al.
Frontiers in Genetics
|
January 23, 2023
Case report: A third variant in the 5' UTR of <i>TWIST1</i> creates a novel upstream translation initiation site in a child with Saethre-Chotzen syndrome
Francisca Diaz-Gonzalez, Javier M Sacedo-Gutiérrez, Stephen R F Twigg, et al.
Clinical Genetics
|
September 30, 2025
Novel MBTPS1 Variants and Cutis Laxa Phenotype in the 8th Reported Case of Spondyloepiphyseal Dysplasia, Kondo-Fu Type
Elsa Lucas-Castro, Francisca Diaz-González, Silvia Modamio-Høybjor, et al.
The Journal of Obstetrics and Gynaecology Research
|
May 15, 2024
Congenital metastatic neuroblastoma with placental involvement as a rare cause of non-immune fetal hydrops
Marta Campillo-Ajenjo, Eva Manuela Pena-Burgos, Beatriz Herrero Ruiz, et al.
Children (Basel, Switzerland)
|
July 29, 2025
Non-Involuting Congenital Hepatic Hemangioma: Lessons from a Case Series
Karla Estefanía-Fernández, Paloma Triana, Carla Ramírez-Amorós, et al.
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Search research articles
Search
Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
European Journal of Medical Genetics
|
March 22, 2021
Description of four patients with TRIP11 variants expand the clinical spectrum of odontochondroplasia (ODCD) and demonstrate the existence of common variants
Mariana Del Pino, Maria José Sanchez-Soler, Manuel Parrón-Pajares, et al.
Archivos De Bronconeumologia
|
September 5, 2006
[High-resolution computed tomography patterns of organizing pneumonia]
Alberto Bravo Soberón, María Isabel Torres Sánchez, Francisco García Río, et al.
American Journal of Medical Genetics. Part A
|
August 29, 2020
Spondyloepiphyseal dysplasia type Stanescu: Expanding the clinical and molecular spectrum of a very rare type II collagenopathy
André M Travessa, Francisca Díaz-González, Teresa Mirco, et al.
Pediatric Transplantation
|
November 3, 2025
Effect of Muscle Mass on Catch-Up Growth After Liver Transplant in Infants With Biliary Atresia
María D Lledín, Manuel Parrón-Pajares, David Andrade-Guerrero, et al.
European Journal of Medical Genetics
|
August 18, 2021
Early clinical and radiological improvement in a young boy with metaphyseal anadysplasia type 2
Samuel Bonilla-Fornés, Lourdes Galán-Ledesma, Pilar Méndez Pérez, et al.
The Pediatric Infectious Disease Journal
|
July 5, 2023
Acute Suppurative Thyroiditis in Children: Clinical Decision-Making
Silvia Gómez, Cristina Mora, Dorleta López de Suso, et al.
Frontiers in Genetics
|
January 23, 2023
Case report: A third variant in the 5' UTR of <i>TWIST1</i> creates a novel upstream translation initiation site in a child with Saethre-Chotzen syndrome
Francisca Diaz-Gonzalez, Javier M Sacedo-Gutiérrez, Stephen R F Twigg, et al.
Clinical Genetics
|
September 30, 2025
Novel MBTPS1 Variants and Cutis Laxa Phenotype in the 8th Reported Case of Spondyloepiphyseal Dysplasia, Kondo-Fu Type
Elsa Lucas-Castro, Francisca Diaz-González, Silvia Modamio-Høybjor, et al.
The Journal of Obstetrics and Gynaecology Research
|
May 15, 2024
Congenital metastatic neuroblastoma with placental involvement as a rare cause of non-immune fetal hydrops
Marta Campillo-Ajenjo, Eva Manuela Pena-Burgos, Beatriz Herrero Ruiz, et al.
Children (Basel, Switzerland)
|
July 29, 2025
Non-Involuting Congenital Hepatic Hemangioma: Lessons from a Case Series
Karla Estefanía-Fernández, Paloma Triana, Carla Ramírez-Amorós, et al.
Page
of 3