Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laura Armas Junco"'
Publikováno v:
Millenium, Vol 2, Iss 24 (2024)
Introducción: El síndrome de Rett es una enfermedad genética que se relaciona con trastornos neurológicos y del desarrollo causados típicamente por mutaciones en el gen MECP2. Afecta principalmente al sexo femenino y puede conducir a graves anom
Externí odkaz:
https://doaj.org/article/814944e140bf49cca4c6690f9763461f
Publikováno v:
INFAD, Vol 3, Iss 1 (2021)
El síndrome de Mayer-Rokitansky-Küster-Hauser (MRKH), comúnmente denominado síndrome de Rokitansky, es una rara anomalía congénita del tracto genital caracterizada por la ausencia de útero y vagina en mujeres fenotípicamente normales. Se cons
Externí odkaz:
https://doaj.org/article/4c057babbf43436ebeec82f890042d0b
Publikováno v:
Children, Vol 9, Iss 2, p 143 (2022)
The high incidence of Type 1 Diabetes Mellitus (DM1) increases the likelihood of teachers having students with this illness in their classrooms. The objective of this study is to investigate the needs of students with DM1 during the school day from t
Externí odkaz:
https://doaj.org/article/4d9dea961e30456e9194bae9abc6e604
Publikováno v:
Children; Volume 9; Issue 2; Pages: 143
The high incidence of Type 1 Diabetes Mellitus (DM1) increases the likelihood of teachers having students with this illness in their classrooms. The objective of this study is to investigate the needs of students with DM1 during the school day from t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c07d71c08d14efe8900862cdc7a9e5a
Publikováno v:
F: Clinical studies: case reports, observational studies and trials.
Background Huntington’s disease (HD) is a hereditary neurodegenerative disorder of the central nervous system. It is transmitted from parents to children, producing emotional and structural changes in family life. It is categorized as a minority di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b4935c61c7319c9c14829e80db76f40
https://doi.org/10.1136/jnnp-2021-ehdn.54
https://doi.org/10.1136/jnnp-2021-ehdn.54
Publikováno v:
INFAD, Vol 3, Iss 1 (2021)
El síndrome de Mayer-Rokitansky-Küster-Hauser (MRKH), comúnmente denominado síndrome de Rokitansky, es una rara anomalía congénita del tracto genital caracterizada por la ausencia de útero y vagina en mujeres fenotípicamente normales. Se cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68d26759aa49cb15710c0bb95e6026be
https://doi.org/10.17060/ijodaep.2021.n1.v3.2036
https://doi.org/10.17060/ijodaep.2021.n1.v3.2036