Works matching DE "FIBRODYSPLASIA ossificans progressiva"
Results: 636
Fibrodisplasia osificante progresiva. Reporte de un caso.
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- Acta Ortopédica Mexicana, 2012, v. 26, n. 3, p. 192
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- Article
Síndrome de fibrodisplasia osificante progresiva (FOP). Informe de tres casos.
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- Acta Ortopédica Mexicana, 2011, v. 25, n. 4, p. 236
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- Article
Editorial highlights.
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- Developmental Dynamics, 2023, v. 252, n. 5, p. 552, doi. 10.1002/dvdy.593
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- Article
Functional comparison of human ACVR1 and zebrafish Acvr1l FOP‐associated variants in embryonic zebrafish.
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- Developmental Dynamics, 2023, v. 252, n. 5, p. 605, doi. 10.1002/dvdy.566
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- Publication type:
- Article
The role of the protein tyrosine phosphatase SHP2 in ossification.
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- Developmental Dynamics, 2022, v. 251, n. 5, p. 748, doi. 10.1002/dvdy.449
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- Publication type:
- Article
Cilia kinases in skeletal development and homeostasis.
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- Developmental Dynamics, 2022, v. 251, n. 4, p. 577, doi. 10.1002/dvdy.426
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- Publication type:
- Article
BMP signaling and skeletal development in fibrodysplasia ossificans progressiva (FOP).
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- Developmental Dynamics, 2022, v. 251, n. 1, p. 164, doi. 10.1002/dvdy.387
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- Publication type:
- Article
Fibrodysplasia ossificans progressiva: when a double skeleton is present.
- Published in:
- 2023
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- Publication type:
- Case Study
Fibrodysplasia (myositis) ossificans progressiva (FOP).
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- 2022
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- Publication type:
- Editorial
Idiopathic dorsal spinal cord herniation perforating the lamina: a case report and review of the literature.
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- Acta Neurochirurgica, 2021, v. 163, n. 8, p. 2313, doi. 10.1007/s00701-021-04804-4
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- Article
Congenital Insensitivity to Pain with Anhidrosis (CIPA) Syndrome; A Rare Genetic Disorder Case Story.
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- Case Reports in Clinical Practice, 2022, v. 7, n. 2, p. 97
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- Publication type:
- Article
Shared Mutation for Two Childhood Diseases.
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- JNCI: Journal of the National Cancer Institute, 2014, v. 106, n. 7, p. 4, doi. 10.1093/jnci/dju222
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- Publication type:
- Article
IN MEMORIAM: ACADEMIC MOMIR POLENAKOVIC, PEDIATRIC NEPHROLOGY, RARE DISEASES AND PUBLISHING IN MACEDONIA.
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- Contributions / Prilozi (1857-9345), 2021, v. 42, n. 2, p. 27, doi. 10.2478/prilozi-2021-0017
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- Publication type:
- Article
Asymptomatic Myositis Ossificans of the Medial Pterygoid Muscles: A Case Report.
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- Journal of Orofacial Pain, 1994, v. 8, n. 2, p. 223
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- Publication type:
- Article
Radiation Therapy in Treatment of Fibrodysplasia Ossificans Progressiva: A Case Report and Review of the Literature.
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- Collegium Antropologicum, 2011, v. 35, n. 2, p. 611
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- Publication type:
- Article
Pigmentary retinal dystrophy associated with peroxisome biogenesis disorder-Zellweger syndrome spectrum.
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- Oxford Medical Case Reports, 2024, v. 2024, n. 6, p. 1, doi. 10.1093/omcr/omae067
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- Publication type:
- Article
Inflammation, immunity, and vascular remodeling in pulmonary hypertension; Evidence for complement involvement?
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- Global Cardiology Science & Practice, 2020, v. 2020, n. 1, p. 1, doi. 10.21542/gcsp.2020.1
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- Publication type:
- Article
[ 18 F]NaF PET/CT as a Marker for Fibrodysplasia Ossificans Progressiva: From Molecular Mechanisms to Clinical Applications in Bone Disorders.
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- Biomolecules (2218-273X), 2024, v. 14, n. 10, p. 1276, doi. 10.3390/biom14101276
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- Article
Molecular Developmental Biology of Fibrodysplasia Ossificans Progressiva: Measuring the Giant by Its Toe.
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- Biomolecules (2218-273X), 2024, v. 14, n. 8, p. 1009, doi. 10.3390/biom14081009
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- Publication type:
- Article
Cell Senescence in Heterotopic Ossification.
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- Biomolecules (2218-273X), 2024, v. 14, n. 4, p. 485, doi. 10.3390/biom14040485
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- Publication type:
- Article
Immunologic Aspects in Fibrodysplasia Ossificans Progressiva.
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- Biomolecules (2218-273X), 2024, v. 14, n. 3, p. 357, doi. 10.3390/biom14030357
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- Publication type:
- Article
Intersections of Fibrodysplasia Ossificans Progressiva and Traumatic Heterotopic Ossification.
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- Biomolecules (2218-273X), 2024, v. 14, n. 3, p. 349, doi. 10.3390/biom14030349
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- Publication type:
- Article
Hedgehog Signaling Controls Chondrogenesis and Ectopic Bone Formation via the Yap-Ihh Axis.
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- Biomolecules (2218-273X), 2024, v. 14, n. 3, p. 347, doi. 10.3390/biom14030347
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- Publication type:
- Article
Sex as a Critical Variable in Basic and Pre-Clinical Studies of Fibrodysplasia Ossificans Progressiva.
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- Biomolecules (2218-273X), 2024, v. 14, n. 2, p. 177, doi. 10.3390/biom14020177
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- Publication type:
- Article
The HIF-1α and mTOR Pathways Amplify Heterotopic Ossification.
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- Biomolecules (2218-273X), 2024, v. 14, n. 2, p. 147, doi. 10.3390/biom14020147
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- Publication type:
- Article
How Activin A Became a Therapeutic Target in Fibrodysplasia Ossificans Progressiva.
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- Biomolecules (2218-273X), 2024, v. 14, n. 1, p. 101, doi. 10.3390/biom14010101
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- Publication type:
- Article
AAV-Mediated Targeting of the Activin A-ACVR1 R206H Signaling in Fibrodysplasia Ossificans Progressiva.
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- Biomolecules (2218-273X), 2023, v. 13, n. 9, p. 1364, doi. 10.3390/biom13091364
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- Article
ISUOG Practice Guidelines (updated): sonographic examination of the fetal central nervous system. Part 2: performance of targeted neurosonography.
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- 2021
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- Publication type:
- journal article
P02.09: Prenatal diagnosis and genetic counselling of FGFR3 gene‐related fetal skeletal dysplasia with analysis of 13 clinical cases.
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- Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 144, doi. 10.1002/uog.19633
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- Publication type:
- Article
OP27.05: In utero diagnosis of fibrodysplasia ossificans progressiva.
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- Ultrasound in Obstetrics & Gynecology, 2014, v. 44, p. 169, doi. 10.1002/uog.13901
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- Publication type:
- Article
Generalized Epileptic Seizures in Fibrodysplasia Ossificans Progressiva Harboring a Recurrent Heterozygous Variant of the ACVR1 Gene (R206H).
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- 2024
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- Publication type:
- Case Study
Rapid Progression of Heterotopic Ossification in Severe Variant of Fibrodysplasia Ossificans Progressiva with p.Arg258Gly in ACVR1: A Case Report and Review of Clinical Phenotypes.
- Published in:
- 2022
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- Publication type:
- Case Study
An Activin Receptor IA/Activin-Like Kinase-2 (R206H) Mutation in Fibrodysplasia Ossificans Progressiva.
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- Case Reports in Genetics, 2013, p. 1, doi. 10.1155/2013/260371
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- Publication type:
- Article
Spinular follicular keratosis of Siemens associated with wooly hair in two sisters: Trichoscopic description and anatomopathological correlation.
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- Our Dermatology Online / Nasza Dermatologia Online, 2022, v. 13, n. 4, p. 449, doi. 10.7241/ourd.20224.22
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- Publication type:
- Article
Diagnostic Findings and Surgical Management of Three Dogs Affected by Osseous Metaplasia Secondary to a Salivary Mucocele.
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- Animals (2076-2615), 2023, v. 13, n. 9, p. 1550, doi. 10.3390/ani13091550
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- Publication type:
- Article
Early Gastric Cancer Concurrent with Gastritis Cystica Profunda Resembling Advanced Cancer.
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- Chonnam Medical Journal, 2024, v. 60, n. 1, p. 87, doi. 10.4068/cmj.2024.60.1.87
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- Publication type:
- Article
A Late Juvenile Onset Type Metachromatic Leukodystrophy Case Presenting With Continuous Pseudobulbar Crying.
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- Cumhuriyet Medical Journal, 2022, v. 44, n. 2, p. 228, doi. 10.7197/cmj.1088934
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- Publication type:
- Article
Displasia tanatofórica tipo II, una entidad congénita inusual. Reporte de caso.
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- Médicas UIS, 2022, v. 35, n. 2, p. 73, doi. 10.18273/revmed.v35n2-2022007
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- Publication type:
- Article
Direct BMP signaling to chordoblasts is required for the initiation of segmented notochord sheath mineralization in zebrafish vertebral column development.
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- Frontiers in Endocrinology, 2023, p. 1, doi. 10.3389/fendo.2023.1107339
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- Publication type:
- Article
Exploration of the skeletal phenotype of the Col1a1<sup>+/Mov13</sup> mouse model for haploinsufficient osteogenesis imperfecta type 1.
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- Frontiers in Endocrinology, 2023, v. 14, p. 01, doi. 10.3389/fendo.2023.1145125
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- Publication type:
- Article
Diffuse Idiopathic Skeletal Hyperostosis: A Case with Dysphonia, Dysphagia and Myelopathy.
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- American Journal of Case Reports, 2019, v. 20, p. 1, doi. 10.12659/AJCR.913792
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- Publication type:
- Article
Non-traumatic myositis ossificans: report of three cases.
- Published in:
- 2014
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- Publication type:
- Abstract
Fibroplasia Ossificans Progressiva: A Case Report of a Rare Disease Entity.
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- Ethiopian Journal of Health Sciences, 2018, v. 28, n. 4, p. 513, doi. 10.4314/ejhs.v28i4.17
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- Publication type:
- Article
FIBRODYSPLASIA OSSIFICANS PROGRESSIVA - RECOGNISING THE EARLY FEATURES AND AVOID DOING HARM.
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- Pediatric Oncall Journal, 2022, v. 19, n. 1, p. 15, doi. 10.7199/ped.oncall.2022.11
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- Publication type:
- Article
FIBROMUSCULAR DYSPLASIA IN A CHILD WITH HYPERTENSION AND STROKE.
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- Pediatric Oncall Journal, 2019, v. 16, n. 3, p. 88, doi. 10.7199/ped.oncall.2019.43
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- Publication type:
- Article
Importance of Recognising Dysmorphic Features: Trichorhinophalangeal Syndrome.
- Published in:
- 2023
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- Publication type:
- Case Study
Heterotopic Ossification at Uncommon Sites: A Case Series of 4 Rare Cases.
- Published in:
- 2024
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- Publication type:
- Case Study
The Revolution in Human Monogenic Disease Mapping.
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- Genes, 2014, v. 5, n. 3, p. 792, doi. 10.3390/genes5030792
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- Publication type:
- Article
An in silico study to find potential effective circRNAs in the progression of Huntington's disease.
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- Iranian Journal of Basic Medical Sciences, 2023, v. 26, n. 8, p. 934, doi. 10.22038/IJBMS.2023.67791.14839
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- Publication type:
- Article
Fibrodysplasia ossificans progressiva: a case report.
- Published in:
- 2016
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- Publication type:
- Case Study