Copertina

Persistencia de movimientos en espejo congénitos en una hemiplejia por infarto cerebral

Fuente: Redalyc

Salvato in:

Dettagli Bibliografici
Autore principale:	Luis Cartier R.
Natura:	Artículo científico
Lingua:	es
Pubblicazione:	Sociedad de Neurología, Psiquiatría y Neurocirugía de Chile 2010
Soggetti:	Medicina sinkinesis Congenital mirror movements Central Pattern Generator Networks
Accesso online:	Acceder al recurso
Tags:	Aggiungi Tag Nessun Tag, puoi essere il primo ad aggiungerne!!

Documenti analoghi

ECMO: Improving our Results by Chasing the Rabbits
di: Luiz Fernando Canêo
Pubblicazione: (2015)

Charaterization of prenatal exposure variables in a group of children aged 0-5 years with congenital heart defect treated in Cali, Colombia. The importance of folic acid
di: Julián Ramírez-Cheyne
Pubblicazione: (2020)

Criss-cross heart: report of two cases, anatomic and surgical description and literature review
di: Ítalo Martins de Oliveira
Pubblicazione: (2013)

Refractory congenital chylous ascites—Case report of a successful surgical management
di: Inês Araújo Oliveira, et al.
Pubblicazione: (2025)

Recommendations for starting a grown up congenital heart disease (GUCH) unit
di: Fernando Tadeu Vasconcelos Amaral
Pubblicazione: (2015)

A Case of HNRNPU ‐Related Neurodevelopmental Disorder Presenting With Acute Encephalopathy and Basal Ganglia Lesions
di: Syunsuke Nagara, et al.
Pubblicazione: (2026)

Severe pharyngeal stenosis and laryngomalacia in an individual of HNRNPU ‐related neurodevelopmental disorder associated with a novel nonsense variant
di: Yusuke Sasaki, et al.
Pubblicazione: (2025)

Non‐Immune Hydrops Fetalis, Multifocal Chorangiomatosis, and Noonan Syndrome 8
di: Eugen‐Matthias Strehle, et al.
Pubblicazione: (2025)

Assisted reproduction and congenital malformations: A systematic review and meta‐analysis
di: Meenakshi Veeramani, et al.
Pubblicazione: (2024)

Morphogenesis of the Extraocular Muscles During the Human Embryonic and Early Fetal Periods
di: Miho Osaka, et al.
Pubblicazione: (2026)

A case series study on the safety of cefditoren pivoxil use during the first trimester of pregnancy in Japan
di: Mariko Honma, et al.
Pubblicazione: (2024)

Acoustic evaluation of voice signal distortion by videoconferencing platforms and devices used in telepractice for cleft palate
di: Shiho Tajiri, et al.
Pubblicazione: (2024)

Questionnaire survey on public awareness of cleft lip with/without palate in Mongolia
di: Anar‐Erdene Gantugs, et al.
Pubblicazione: (2024)

Postnatal Bimodal Dynamics and Androgen‐Induced Masculinization of the External Genitalia in Mice
di: Junki Aikawa, et al.
Pubblicazione: (2026)

Urinary Metabolic Screening Misled the Molecular Diagnosis of Xia–Gibbs Syndrome
di: Sayaka Enomoto, et al.
Pubblicazione: (2026)

Risk of major birth defects after first‐trimester exposure to carbocisteine and ambroxol: A multicenter prospective cohort study using counseling data for drug safety during pregnancy
di: Mariko Usuda, et al.
Pubblicazione: (2024)

Morphological relationship between the cranial base and facial anomalies in humans: Challenges and future perspectives
di: Natsuko Utsunomiya, et al.
Pubblicazione: (2025)

Predictability of fetal pulmonary artery Doppler on neonatal outcomes in pregnant women with gestational diabetes mellitus
di: Huriye Ezveci, et al.
Pubblicazione: (2025)

Compound heterozygous ZNF335 variants in a patient with microcephaly, refractory epilepsy, and severe developmental delay: A case report and literature review
di: Kaori Yamoto, et al.
Pubblicazione: (2025)

Risk factors for isolated congenital heart defects in infants from Western Mexico
di: Jessica Paola Cruz‐Cruz, et al.
Pubblicazione: (2024)

Pyramidalis muscle formation during human embryonic and early fetal periods
di: Yui Iwasa, et al.
Pubblicazione: (2024)

Co‐Occurrence of Urogenital Anomalies and Congenital Heart Disease in a Child With Alpha‐Thalassemia Mental Retardation Syndrome Associated With Chromosome 16 Abnormalities due to Partial Monosomy 16p13.3 and Partial Trisomy 16q22.1–q24.3
di: Hideki Tamaru, et al.
Pubblicazione: (2025)

Focused Clinical Observation of Functional Outcomes in Children With OEIS Complex
di: Osamu Yazawa, et al.
Pubblicazione: (2026)

A cohort study on structural analysis of congenital anomalies in an intensive care unit in Azerbaijan
di: Narmin Akif Azizova, et al.
Pubblicazione: (2025)

Patients With Hereditary Hemorrhagic Telangiectasia Diagnosed by Nanopore Long Read Sequencer
di: Mamiko Yamada, et al.
Pubblicazione: (2025)

Cervical vertebrae fusion in elbow knee synostosis ( Eks )‐mutant mice with fibroblast growth factor 9 N143T mutation
di: Georgina Djameh, et al.
Pubblicazione: (2025)

Revisiting ultrasonographic soft markers of aneuploidy: A thoughtful analysis in low‐risk and screening naïve Indian antenatal women
di: Shreya Das, et al.
Pubblicazione: (2025)

Correction to “Cohort Study of Pregnancy Outcomes After Exposure to Fexofenadine or Olopatadine in the First Trimester”
Pubblicazione: (2026)

A C ‐Propeptide Variant in COL1A1 Potentially Perturbing Disulfide Bonding in Osteogenesis Imperfecta Type III
di: Daisuke Watanabe, et al.
Pubblicazione: (2026)

Correction to: “Patterns of Primary and Secondary Defects Associated With Non‐Syndromic Cleft Lip and Palate: An Epidemiological Analysis in a Kenyan Population”
Pubblicazione: (2025)

Congenital cardiac anomalies in non‐syndromic cleft lip and cleft palate patients: A systematic review and meta‐analysis
di: Bindey Kumar, et al.
Pubblicazione: (2024)

Cohort Study of Pregnancy Outcomes After Exposure to Fexofenadine or Olopatadine in the First Trimester
di: Kaori Yamazaki, et al.
Pubblicazione: (2026)

Upper airway obstruction due to congenital epiglottic cyst: Report of two cases
di: Kensuke Uraguchi, et al.
Pubblicazione: (2024)

The Japanese Teratology Society 65th Annual Meeting July 25–27, 2025
Pubblicazione: (2025)

Improvement of speech function in submucous cleft palate through conservative treatment
di: Nagana Natsume, et al.
Pubblicazione: (2025)

The role of sonic hedgehog signaling in the oropharyngeal epithelium during jaw development
di: Rika Takeuchi, et al.
Pubblicazione: (2024)

Accumulation of ether phospholipids in induced pluripotent stem cells and oligodendrocyte‐lineage cells established from patients with Sjögren‐Larsson syndrome
di: Yu Yamaguchi, et al.
Pubblicazione: (2024)

Refining the Neonatal Phenotypic Spectrum of Distal Deletion 14q Syndrome: Early Genomic Diagnosis in Infancy
di: Koji Nakae, et al.
Pubblicazione: (2026)

Issue Information
Pubblicazione: (2024)

Ultrasound and magnetic resonance imaging features of fetal urogenital anomalies: A pictorial essay
di: Behnaz Moradi, et al.
Pubblicazione: (2024)