Clinical and Molecular Features of Patients With Congenital Disorders of Glycosylation in Japan by Nobuhiko Okamoto, Machiko Kadoya, Yoshinao Wada

Subjects: “…ATP6V0A2‐CDG…”
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Glycosphingolipid synthesis is impaired in SLC35A2-CDG and improves with galactose supplementation by Andrea Jáñez Pedrayes, Sam De Craemer, Jakub Idkowiak, Dries Verdegem, Christian Thiel, Rita Barone, Mercedes Serrano, Tomáš Honzík, Eva Morava, Pieter Vermeersch, François Foulquier, Willy Morelle, Johannes V. Swinnen, Daisy Rymen, David Cassiman, Bart Ghesquière, Peter Witters

Subjects: “…CDG…”
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The long way to diagnosis: attention disorder, alcohol addiction or congenital disorder of glycosylation? A case report by Timo Jendrik Faustmann, Lukas Hensel, Armin Bahic, Yoshinao Wada, Marianne Grüneberg, Thorsten Marquardt, Daniel Kamp, Leonhard Schilbach

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Evaluation of the effects of Chinese Dietary Guidelines on nutrition, environment, and cost by Shunan Zhao, Rui Li, Meng Li, Yanan Wang, Juan Wang, Rong Yuan

Subjects: “…Chinese Dietary Guidelines (CDG)…”
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PMM2-CDG T237M Mutation in a Patient with Cerebral Palsy-Like Phenotypes Reported from South India by N. Sreedevi, N. Swapna, Santosh Maruthy, H.S. Meghavathi, Charles Sylvester

Subjects: “…pmm2-cdg…”
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<i>In Silico</i> Analysis of Phosphomannomutase-2 Dimer Interface Stability and Heterodimerization with Phosphomannomutase-1 by Bruno Hay Mele, Jessica Bovenzi, Giuseppina Andreotti, Maria Vittoria Cubellis, Maria Monticelli

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Two novel cases with PIGQ-CDG: expansion of the genotype–phenotype spectrum and evaluation of GestaltMatcher as a diagnostic tool by Katarína Kušíková, Tzung-Chien Hsieh, Mateja Pfeifer, Christine Fauth, Yoshiko Murakami, Franco Laccone, Daniela Karall, Walter Bonfig, Helen Stewart, Denisa Weis

Subjects: “…PIGQ-CDG…”
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Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders by Sebile Kılavuz, Fatma Derya Bulut, Deniz Kor, Berna Şeker Yılmaz, Atıl Bişgin, Fadli Demir, Bahriye Atmış, Derya Alabaz, Neslihan Mungan, Mustafa Yılmaz

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A comprehensive update of genotype–phenotype correlations in PMM2-CDG: insights from molecular and structural analyses by Tiago Oliveira, Ricardo Ferraz, Luísa Azevedo, Dulce Quelhas, João Carneiro, Jaak Jaeken, Sérgio F. Sousa

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Microwave-assisted synthesis and swelling behavior of poly lactic acid (PLA) grafted Cordia dichotoma gum-based hydrogels by Jyoti Sinha, Abubakar Hamisu Mijinyawa, Faisal Islam Chowdhury, Muhd Zu Azhan Yahya, Pramod Kumar Singh, Geeta Durga

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Integrability, Hirota D-operator expression, multi solitons, breather wave, and complexiton of a generalized Korteweg-de Vries–Caudrey Dodd Gibbon equation by Kamyar Hosseini, Farzaneh Alizadeh, Sekson Sirisubtawee, Chaiyod Kamthorncharoen, Samad Kheybari, Kaushik Dehingia

Subjects: “…gkdv–cdg equation…”
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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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