El síndrome de Loeys – Dietz
REDOE - Revista Europea de Odontoestomatologia
Loeys-Dietz syndrome: MedlinePlus Genetics
IJERPH | Free Full-Text | How to Distinguish Marfan Syndrome from Marfanoid Habitus in a Physical Examination—Comparison of External Features in Patients with Marfan Syndrome and Marfanoid Habitus
Vista de Manifestaciones cardiovasculares en el síndrome de Ehlers-Danlos tipo hipermóvil | Revista Peruana de Investigación en Salud
Ellas opinan: SuperAina y el síndrome de Loeys-Dietz
JCM | Free Full-Text | Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome
Qué consideramos una cardiopatía familiar?
Activation of TGF-β signaling in an aortic aneurysm in a patient with Loeys- Dietz syndrome caused by a novel loss-of-function variant of TGFBR1 | Human Genome Variation
Severity of oro-dental anomalies in Loeys-Dietz syndrome segregates by gene mutation | Journal of Medical Genetics
Study Characterizes Oro-Dental Anomalies in Loeys-Dietz Syndrome
El síndrome de Loeys – Dietz
Síndromes de Ehlers-Danlos - ANSEDH
Table 3 from Prevalence of Intracranial Aneurysms in Patients with Connective Tissue Diseases: A Retrospective Study | Semantic Scholar
Evaluation of cervical spine pathology in children with Loeys-Dietz syndrome - Surgical Neurology International
Loeys-Dietz Syndrome Foundation - Care Based Upon Strong Facts 💙 Keep reading to hear from our friend, Dr. Dietz! "I was initially trained as a pediatrician and a cardiologist. I was quite
Frontiers | Identification of a Pathogenic TGFBR2 Variant in a Patient With Loeys–Dietz Syndrome
Miguel Marcos on Twitter: "Diagnóstico diferencial de la inflamación de la arteria aorta o aortitis (sí, también puede inflamarse) #FMedUsal #41SEMI" / Twitter
Loeys-Dietz Syndrome on Twitter: "Seasons Change, and I Have Hope! https://t.co/M9hfV3wAJL https://t.co/ZZduHuZzma" / Twitter
Neonatal presentation of Loeys-Dietz syndrome: two case reports and review of the literature | Italian Journal of Pediatrics | Full Text
Hand and fibrillin‐1 deposition abnormalities in Loeys–Dietz syndrome—expanding the clinical spectrum - Chung - 2014 - American Journal of Medical Genetics Part A - Wiley Online Library
Clinical and genetic data of 22 new patients with SMAD3 pathogenic variants and review of the literature. - Abstract - Europe PMC
Neonatal presentation of Loeys-Dietz syndrome: two case reports and review of the literature | Italian Journal of Pediatrics | Full Text
Oral health-related quality of life in Loeys-Dietz syndrome, a rare connective tissue disorder: an observational cohort study | Orphanet Journal of Rare Diseases | Full Text
Loeys-Dietz and Shprintzen-Goldberg syndromes: analysis of TGF-β-opathies with craniofacial manifestations using an innovative multimodality method | Journal of Medical Genetics
Loeys-Dietz syndrome: MedlinePlus Genetics
