Caregiver burden and associated factors among primary caregivers of children with congenital disorders: a comparative cross-sectional study in Hunan Province, China by Yi Yu, Long Yang, Yanlin Liu, Junqun Fang, Hua Wang, Dan Luo

Subjects: “…Congenital disorders…”
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An Exoskeleton Design and Numerical Characterization for Children with Duchenne Muscular Dystrophy by Cristian Copilusi, Sorin Dumitru, Nicolae Dumitru, Ionuț Geonea, Cristian Mic

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The impact of COVID-19 on patients affected by rare diseases and congenital disorders in South Africa: A scoping review by M C M Gomes, H L Malherbe

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Epidemiological and Histopathological Characteristics of Fetuses with Congenital Disorders: A Study in Greece by Despoina Nteli, Maria Nteli, Konstantinos Konstantinidis, Maria Ouzounidou, Paschalis Theotokis, Maria-Eleni Manthou, Iasonas Dermitzakis, Xeni Miliara, Chrysoula Gouta, Stamatia Angelidou, Dimosthenis Miliaras, Soultana Meditskou

Subjects: “…congenital disorders…”
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Combination of general anesthesia and caudal block in laparoscopic surgery for neonates with annular pancreas: A case report by Putu Kurniyanta, Adinda Putri Antasari, Adinda Putra Pradhana

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COG6‐related prenatal phenotype (CDG2L): Clinico‐pathological report and review of the literature by Sarah Guterman, Agnese Feresin, Lucile Boutaud, Clémence Jacquin, Stanislas Lyonnet, Jean‐Pierre Bernard, Claire Colmant, Philippe Roth, Nicolas Bourgon, Pierre Mace, Alice Thoreau, Yves Ville, Joana Bengoa, Zaina Ait Arkoub, Cécile Fourrage, Ferechté Encha‐Razavi, Bettina Bessières, Tania Attié‐Bitach

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Congenital disorders of glycosylation in children – Histopathological and ultrastructural changes in the liver by Patryk Lipiński, Joanna Cielecka-Kuszyk, Elżbieta Czarnowska, Anna Bogdańska, Piotr Socha, Anna Tylki-Szymańska

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Review and metabolomic profiling of unsolved case reveals newly reported autosomal dominant congenital disorder of glycosylation, type Iw formerly thought to only be an autosomal r... by Kimberly M. Ezell, Yutaka Furuta, Devin Oglesbee, Eniko K. Pivnick, David Rinker, Jonathan H. Sheehan, Rory J. Tinker, Rizwan Hamid, Joy D. Cogan, Lynette Rives, Serena Neumann, Brian Corner, Mary Koziura, John A. Phillips, III

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Pediatric Anesthetic Management of a Patient With an ALG‐13 Gene Mutation, a Rare Congenital Disorder of Glycosylation by Esha Thakkar, John A. Iasiello, Sunny R. Cai, Adrienne Hutton

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Structural and Functional Characterization of N-Glycanase-1 Pathogenic Variants by Antje Banning, Lukas Hoeren, Isis Atallah, Ralph Orczyk, David Jacquier, Diana Ballhausen, Ritva Tikkanen

Subjects: “…congenital disorders of deglycosylation…”
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Are viral vector-mediated therapies compatible with aberrant glycosylation? by I.J.J. Muffels, R. Budhraja, S. Radenkovic, R. Shah, A. Pandey, E. Morava, T. Kozicz

Subjects: “…congenital disorders of glycosylation…”
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Congenital Disorders of genital organs with menstrual Blood outflow Defect: Diagnostics, Treatment and Prevention of Complications by Zalina K. Batyrova, E. V. Uvarova, Zaira Kh. Kumykova, Vladimir D. Chuprynin, Diana A. Kruglyak

Subjects: “…congenital disorders…”
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Novel mutation and severe respiratory failure in congenital disorders of glycosylation Type Ix by Betül Kılıç, Nejmiye Akkuş

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Inherited glycosylphosphatidylinositol deficiency disorders: a new group of inherited metabolic disorders by Michał Patalan, Alicja Leśniak, Justyna Paprocka, Agnieszka Zubkiewicz-Kucharska, Kaja Giżewska-Kacprzak, Marta Glińska, Lidia Babiak-Choroszczak, Maria Giżewska, Robert Śmigiel

Subjects: “…congenital disorders of glycosylation…”
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Outcome of creatine supplementation therapy in phosphoglucomutase-1 deficiency associated congenital disorders of glycosylation: Novel insights by Anastasia Ambrose, Morganne McCabe, Clara Hung, Iveta Sosova, Peter Seres, Saadet Mercimek-Andrews

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Mapping the diagnostic odyssey of congenital disorders of glycosylation (CDG): insights from the community by Pedro Granjo, Carlota Pascoal, Diana Gallego, Rita Francisco, Jaak Jaeken, Tristen Moors, Andrew C. Edmondson, Kristin A. Kantautas, Mercedes Serrano, Paula A. Videira, Vanessa dos Reis Ferreira

Subjects: “…Congenital disorders of glycosylation (CDG)…”
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An ALG12-CDG patient with a novel homozygous intronic mutation associated with low ALG12 mRNA by Sandrine Vuillaumier-Barrot, Thierry Dupré, Tiffany Andriantsihoarana, Vincent Desportes, David Cheillan, Stuart E. H. Moore, Isabelle Chantret

Subjects: “…Congenital Disorders of Glycosylation…”
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ALG1-congenital disorder of glycosylation: report of clinical and genetic features of three new cases and review of literature by Faeze Khaghani, Nafiseh Pourbadakhshan, Ehsan Ghayoor Karimiani, Farah Ashrafzadeh, Peyman Eshraghi

Subjects: “…Congenital disorder of glycosylation…”
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Middle-aged Man with Deformities, Discomfort in the Chest, and Dextrocardia by Sriram Veeraraghavan, MD, DM, Bharath Raj Kidambi, MD, DM, Karthikeyan Balakrishnan, MD, DM

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Cognition and behavior in adults with neurofibromatosis type 1 by Anja Bos-Roubos, Anja Bos-Roubos, Anja Bos-Roubos, Hanneke van Leeuwen, Hanneke van Leeuwen, Hanneke van Leeuwen, Ellen Wingbermühle, Ellen Wingbermühle, Ellen Wingbermühle, Ellen Wingbermühle, Louisa van den Bosch, Lindsey Ossewaarde, Walter Taal, Walter Taal, Laura de Graaff, Laura de Graaff, Laura de Graaff, Jos Egger, Jos Egger, Jos Egger, Jos Egger, Jos Egger

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