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JMIR Research Protocols
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June 7, 2022
Hearing Loss in Patients With Morquio Syndrome: Protocol for a Scoping Review
Lorena Diaz-Ordoñez, Estephania Candelo, Katherine Silva-Cuero, et al.
Andes Pediatrica : Revista Chilena De Pediatria
|
January 6, 2025
[Next generation sequencing in pediatric bone marrow failure: a valuable tool for accurate diagnosis]
Rafael Adrián Pacheco-Orozco, Angela Devia, Eliana Manzi, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
February 22, 2019
Paraganglioma in pregnancy: interdisciplinary management during pregnancy
Albaro J Nieto, Lizette Trochez, Daniela Ramírez, et al.
Clinical Neurophysiology Practice
|
February 27, 2026
Symptomatic palatal myoclonus as a rare manifestation of neuro-behcet́s disease: A case report
Andrés Hormaza-Jaramillo, Valentina Quintana-Peña, Harry Pachajoa, et al.
The Application of Clinical Genetics
|
June 9, 2021
The Oral Health of Patients with DiGeorge Syndrome (22q11) Microdeletion: A Case Report
Estephania Candelo, Maria Alejandra Estrada-Mesa, Adriana Jaramillo, et al.
Biomedica : Revista Del Instituto Nacional De Salud
|
July 30, 2024
Genetic and radiological aspects of pediatric renal cystic disease: A case series
Rafael Adrián Pacheco-Orozco, Jessica María Forero-Delgadillo, Vanessa Ochoa, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
May 13, 2021
Genetic and congenital disorders in pre-Hispanic Moche pottery
Harry Pachajoa, Thomas Heyne, Estephania Candelo, et al.
The Application of Clinical Genetics
|
August 24, 2019
First report case with negative genetic study (array CGH, exome sequencing) in patients with vertical transmission of Zika virus infection and associated brain abnormalities
Estephania Candelo, Gabriela Caicedo, Fernando Rosso, et al.
Children (Basel, Switzerland)
|
January 21, 2023
Systemic Bevacizumab for Recurrent Respiratory Papillomatosis: A Scoping Review from 2009 to 2022
Laura Torres-Canchala, Daniela Cleves-Luna, Oriana Arias-Valderrama, et al.
The Application of Clinical Genetics
|
February 19, 2026
Variable Expressivity in Type 2 Familial Partial Lipodystrophy Related to a Pathogenic <i>LMNA</i> Variant R482: Maternal Transmission to Non-Identical Twins
Paola Andrea Duque-Cordoba, Lorena Diaz-Ordoñez, Laura Carvajal-Del-Castillo, et al.
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of 13
Search research articles
Search
Showing results (71-80 of 126) with videos related to
Sort By:
Page
of 13
JMIR Research Protocols
|
June 7, 2022
Hearing Loss in Patients With Morquio Syndrome: Protocol for a Scoping Review
Lorena Diaz-Ordoñez, Estephania Candelo, Katherine Silva-Cuero, et al.
Andes Pediatrica : Revista Chilena De Pediatria
|
January 6, 2025
[Next generation sequencing in pediatric bone marrow failure: a valuable tool for accurate diagnosis]
Rafael Adrián Pacheco-Orozco, Angela Devia, Eliana Manzi, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
February 22, 2019
Paraganglioma in pregnancy: interdisciplinary management during pregnancy
Albaro J Nieto, Lizette Trochez, Daniela Ramírez, et al.
Clinical Neurophysiology Practice
|
February 27, 2026
Symptomatic palatal myoclonus as a rare manifestation of neuro-behcet́s disease: A case report
Andrés Hormaza-Jaramillo, Valentina Quintana-Peña, Harry Pachajoa, et al.
The Application of Clinical Genetics
|
June 9, 2021
The Oral Health of Patients with DiGeorge Syndrome (22q11) Microdeletion: A Case Report
Estephania Candelo, Maria Alejandra Estrada-Mesa, Adriana Jaramillo, et al.
Biomedica : Revista Del Instituto Nacional De Salud
|
July 30, 2024
Genetic and radiological aspects of pediatric renal cystic disease: A case series
Rafael Adrián Pacheco-Orozco, Jessica María Forero-Delgadillo, Vanessa Ochoa, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
May 13, 2021
Genetic and congenital disorders in pre-Hispanic Moche pottery
Harry Pachajoa, Thomas Heyne, Estephania Candelo, et al.
The Application of Clinical Genetics
|
August 24, 2019
First report case with negative genetic study (array CGH, exome sequencing) in patients with vertical transmission of Zika virus infection and associated brain abnormalities
Estephania Candelo, Gabriela Caicedo, Fernando Rosso, et al.
Children (Basel, Switzerland)
|
January 21, 2023
Systemic Bevacizumab for Recurrent Respiratory Papillomatosis: A Scoping Review from 2009 to 2022
Laura Torres-Canchala, Daniela Cleves-Luna, Oriana Arias-Valderrama, et al.
The Application of Clinical Genetics
|
February 19, 2026
Variable Expressivity in Type 2 Familial Partial Lipodystrophy Related to a Pathogenic <i>LMNA</i> Variant R482: Maternal Transmission to Non-Identical Twins
Paola Andrea Duque-Cordoba, Lorena Diaz-Ordoñez, Laura Carvajal-Del-Castillo, et al.
Page
of 13