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Biotechnology Letters
|
January 23, 2026
High-cell-density cultivation of Vibrio natriegens N5.3 on chitin monomers: a step toward chitin valorization
Tuan Le, Thanh-Hung Nguyen, Duc-Chien Vu, et al.
Pediatric Blood & Cancer
|
July 17, 2019
Metastatic neuroblastoma in a patient with ROHHAD: A new alert regarding the risk of aggressive malignancies in this rare condition
Charlotte Calvo, Caroline Storey, Guillaume Morcrette, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 12, 2008
Chiari type I malformation causing central apnoeas in a 4-month-old boy
Mieke J A Van den Broek, Anne-Sophie Arbues, François Chalard, et al.
American Journal of Human Genetics
|
January 20, 2005
PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome
Delphine Trochet, Louise M O'Brien, David Gozal, et al.
Nature Genetics
|
March 18, 2003
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome
Jeanne Amiel, Béatrice Laudier, Tania Attié-Bitach, et al.
Frontiers in Pediatrics
|
September 19, 2022
ROHHAD syndrome without rapid-onset obesity: A diagnosis challenge
Blandine Desse, Antoine Tran, Mathilde Butori, et al.
Orphanet Journal of Rare Diseases
|
May 1, 2015
Proceedings of the fourth international conference on central hypoventilation
Ha Trang, Jean-François Brunet, Hermann Rohrer, et al.
Breathe (Sheffield, England)
|
August 26, 2015
Introducing a core curriculum for respiratory sleep practitioners
Sharon Mitchell, Anita Simonds, Stefan Andreas, et al.
The European Respiratory Journal
|
November 7, 2015
Obstructive sleep disordered breathing in 2- to 18-year-old children: diagnosis and management
Athanasios G Kaditis, Maria Luz Alonso Alvarez, An Boudewyns, et al.
Orphanet Journal of Rare Diseases
|
September 22, 2020
Guidelines for diagnosis and management of congenital central hypoventilation syndrome
Ha Trang, Martin Samuels, Isabella Ceccherini, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
Biotechnology Letters
|
January 23, 2026
High-cell-density cultivation of Vibrio natriegens N5.3 on chitin monomers: a step toward chitin valorization
Tuan Le, Thanh-Hung Nguyen, Duc-Chien Vu, et al.
Pediatric Blood & Cancer
|
July 17, 2019
Metastatic neuroblastoma in a patient with ROHHAD: A new alert regarding the risk of aggressive malignancies in this rare condition
Charlotte Calvo, Caroline Storey, Guillaume Morcrette, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 12, 2008
Chiari type I malformation causing central apnoeas in a 4-month-old boy
Mieke J A Van den Broek, Anne-Sophie Arbues, François Chalard, et al.
American Journal of Human Genetics
|
January 20, 2005
PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome
Delphine Trochet, Louise M O'Brien, David Gozal, et al.
Nature Genetics
|
March 18, 2003
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome
Jeanne Amiel, Béatrice Laudier, Tania Attié-Bitach, et al.
Frontiers in Pediatrics
|
September 19, 2022
ROHHAD syndrome without rapid-onset obesity: A diagnosis challenge
Blandine Desse, Antoine Tran, Mathilde Butori, et al.
Orphanet Journal of Rare Diseases
|
May 1, 2015
Proceedings of the fourth international conference on central hypoventilation
Ha Trang, Jean-François Brunet, Hermann Rohrer, et al.
Breathe (Sheffield, England)
|
August 26, 2015
Introducing a core curriculum for respiratory sleep practitioners
Sharon Mitchell, Anita Simonds, Stefan Andreas, et al.
The European Respiratory Journal
|
November 7, 2015
Obstructive sleep disordered breathing in 2- to 18-year-old children: diagnosis and management
Athanasios G Kaditis, Maria Luz Alonso Alvarez, An Boudewyns, et al.
Orphanet Journal of Rare Diseases
|
September 22, 2020
Guidelines for diagnosis and management of congenital central hypoventilation syndrome
Ha Trang, Martin Samuels, Isabella Ceccherini, et al.
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of 5