12 results on '"JUANES, MATÍAS"'
Search Results
2. Molecular diagnosis of epileptic encephalopathy of the first year of life applying a customized gene panel in a group of Argentinean patients
3. De novo absence status epilepticus associated with the SLC6A1 gene in a pediatric patient
4. THU157 Epigenetic Regulation Of Genes Involved In The Signaling Cascade Of The GH Axis - IGF1 And Insulin. Implication In Children Postnatal Growth
5. Dravet Syndrome: An Electroclinical, Genetic, Treatment, and Outcome Study of 35 Patients in Argentina
6. De novo absence status epilepticus associated with the SLC6A1gene in a pediatric patient
7. Five New Cases of 46,XX Aromatase Deficiency: Clinical Follow-Up From Birth to Puberty, a Novel Mutation, and a Founder Effect
8. CLINICAL AND GENETIC STUDY OF DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY IN ARGENTINEAN PEDIATRIC PATIENTS.
9. Next Generation Sequencing-Based Mutational Profile of Therapy-Related AML and De Novo AML: Results from a Single Pediatric Institution in Argentina
10. Presence of GH1 and absence of GHRHR gene mutations in a large cohort of Argentinian patients with severe short stature and isolated GH deficiency
11. TWO NOVEL HETEROZYGOUS MISSENSE VARIATIONS WITHIN THE GLI2 GENE IN TWO UNRELATED ARGENTINE PATIENTS.
12. De novo absence status epilepticus associated with the SLC6A1 gene in a pediatric patient.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.