Hasil Pencarian - Catarina Limbert

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  1. 1
    Hypogonadotropic hypogonadism due to compound heterozygous mutations TACR3 in siblings

    Hypogonadotropic hypogonadism due to compound heterozygous mutations TACR3 in siblings oleh Rita Valsassina, Filipa Briosa, Joana Soares, Marta Amorim, Catarina Limbert

    Diterbitkan 2020-12-01
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  2. 2
    The rare DRB1*04:08-DQ8 haplotype is the main HLA class II genetic driver and discriminative factor of Early-onset Type 1 diabetes in the Portuguese population

    The rare DRB1*04:08-DQ8 haplotype is the main HLA class II genetic driver and discriminative factor of Early-onset Type 1 diabetes in the Portuguese population oleh Iris Caramalho, Iris Caramalho, Paula Matoso, Dário Ligeiro, Tiago Paixão, Daniel Sobral, Ana Laura Fitas, Catarina Limbert, Catarina Limbert, Jocelyne Demengeot, Carlos Penha-Gonçalves

    Diterbitkan 2024-01-01
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  3. 3
    Do GnRH Agonists Really Increase Body Weight Gain? Evaluation of a Multicentric Portuguese Cohort of Patients With Central Precocious Puberty

    Do GnRH Agonists Really Increase Body Weight Gain? Evaluation of a Multicentric Portuguese Cohort of Patients With Central Precocious Puberty oleh Ana Luísa Leite, Elisa Galo, Ana Antunes, Brígida Robalo, Brígida Robalo, Daniela Amaral, Filipa Espada, Sofia Castro, Sara Simões Dias, Sara Simões Dias, Catarina Limbert, Catarina Limbert

    Diterbitkan 2022-03-01
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  4. 4
    Diplopia, Convergent Strabismus, and Eye Abduction Palsy in a 12-Year-Old Boy with Autoimmune Thyroiditis

    Diplopia, Convergent Strabismus, and Eye Abduction Palsy in a 12-Year-Old Boy with Autoimmune Thyroiditis oleh Pedro Marques, Sandra Jacinto, Maria do Carmo Pinto, Catarina Limbert, Lurdes Lopes

    Diterbitkan 2016-01-01
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  5. 5
    Pesquisa de sequências do cromossoma Y em indivíduos com síndroma de Turner.

    Pesquisa de sequências do cromossoma Y em indivíduos com síndroma de Turner. oleh Lénia Ferrão, Maria Lurdes Lopes, Catarina Limbert, Bárbara Marques, Filomena Boieiro, Marisa Silva, Ramira Marques, João Lavinha, Amilcar Mota, João Gonçalves

    Diterbitkan 2002-04-01
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  6. 6
    Whole Exome Sequencing in Children With Type 1 Diabetes Before Age 6 Years Reveals Insights Into Disease Heterogeneity

    Whole Exome Sequencing in Children With Type 1 Diabetes Before Age 6 Years Reveals Insights Into Disease Heterogeneity oleh Andreia Fiúza Ribeiro, Ana Laura Fitas, Marcela Oliveira Pires, Paula Matoso, Dário Ligeiro, Daniel Sobral, Carlos Penha-Gonçalves, Jocelyne Demengeot, Íris Caramalho, Catarina Limbert

    Diterbitkan 2024-01-01
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