অনুসন্ধান ফলাফলগুলি - Charles Marques Lourenço
- প্রদর্শন 1 - 20 ফলাফল এর 132
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Epilepsy in mucopolysaccharidosis disorders অনুযায়ী Maurizio Scarpa, Charles Marques Lourenço, Hernán Amartino
প্রকাশিত 2017Revisão -
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Analysis of the caregiver burden associated with Sanfilippo syndrome type B: panel recommendations based on qualitative and quantitative data অনুযায়ী Elsa Shapiro, Charles Marques Lourenço, Neslihan Önenli Mungan, Nicole Muschol, Cara O’Neill, Suresh Vijayaraghavan
প্রকাশিত 2019Artigo -
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1067 Safety of Substrate Reduction Terapy in a Toddler with Niemann-Pick Typec Disease: A Case Report অনুযায়ী José Simon Camelo, Charles Marques Lourenço, Wilson Marques, Marlene Turcato, Carolina A. R. Funayama, Regina Sawamura, Mariana Fernandes
প্রকাশিত 2010Artigo -
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Fifteen years of enzyme replacement therapy for mucopolysaccharidosis type VI (Maroteaux–Lamy syndrome): a case report অনুযায়ী Isadora Andrade, River Ribeiro, Zumira Aparecida Carneiro, Roberto Giugliani, Catarina Pereira, Claudia Cozma, Daniel Grinberg, Lluı̈sa Vilageliu, Charles Marques Lourenço
প্রকাশিত 2022Artigo -
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P015: Connecting the dots (and neurons): Unraveling the genetic basis of neurotransmitters disorders in a large cohort of Brazilian patients অনুযায়ী Charles Marques Lourenço, Amadeu Queiroz, Lilian Sansão, Regina Albuquerque, Jacqueline Fonseca, Érica Coelho, Maria da Penha Ananias Morita, Eduardo Estephan
প্রকাশিত 2024Artigo -
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Widening the clinical spectrum of Pitt-Rogers-Danks/Wolf-Hirschhorn syndromes অনুযায়ী Juliana F. Mazzeu, Ana Cristina Victorino Krepischi, Carla Rosenberg, Charles Marques Lourenço, Karina Lezirovitz, Károly Szuhai, Lúcia Martelli, Angela Maria Vianna‐Morgante
প্রকাশিত 2007Artigo -
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Analyses of disease-related GNPTAB mutations define a novel GlcNAc-1-phosphotransferase interaction domain and an alternative site-1 protease cleavage site অনুযায়ী Renata Voltolini Velho, Raffaella De Pace, Sarah Klünder, Fernanda Sperb‐Ludwig, Charles Marques Lourenço, Ida Vanessa Döederlein Schwartz, Thomas Braulke, Sandra Pohl
প্রকাশিত 2015Artigo
অনুসন্ধান সাধনীগুলি:
সম্পর্কিত বিষয়
Medicine
Biology
Genetics
Gene
Internal medicine
Disease
Phenotype
Pathology
Mutation
Pediatrics
Biochemistry
Neuroscience
Psychiatry
Bioinformatics
Enzyme replacement therapy
Gastroenterology
Missense mutation
Ataxia
Chemistry
Exome sequencing
Genetic heterogeneity
Niemann–Pick disease, type C
Enzyme
Epilepsy
Hereditary spastic paraplegia
Lysosomal storage disease
Mucopolysaccharidosis
Psychology
Allele
Amino acid