Results 111 to 120 of about 6,213,342 (156)

Dual-Targeted Therapy in Refractory Pyoderma Gangrenosum: A Focused Systematic Review of Convergent Pathway Targeting. [PDF]

Dermatol Ther (Heidelb)
Shanshal M, Karanasios G.
europepmc   +1 more source

Hereditary connective tissue disorders in unselected patients with spontaneous cervical artery dissection: a targeted next generation sequencing approach and systematic review. [PDF]

Neurol Sci
Corradi L, Ferraro C, Tesi F, Abrignani G, Castellini P, Latte L, Trapasso MC, Genovese A, Ritelli MG, Cinquina V, Giliani SC, Magoni M, Menozzi R, Pezzini A.   +13 more
europepmc   +1 more source

Sclerosing bone dysplasias: a pictorial essay. [PDF]

Radiol Bras
Galdino VAC, Martins MM, Marcos VN, Gonçalves GF, Dias RG, Mileti DR.   +5 more
europepmc   +1 more source

Camurati-Engelmann disease (diaphyseal dysplasia)

, 2013
openaire   +1 more source

Camurati-Engelmann Disease. Effects of Corticosteroids

Acta Clinica Belgica, 1998
Camurati-Engelmann disease is an uncommon condition, radiologically characterized by symmetric diaphyseal sclerosis involving the tubular bones. Clinical features include limb pain, muscle weakness, waddling gait and sometimes deafness. The evaluation is made by conjunction of radiographic and scintigraphic data.
Heymans, Olivier, Gebhart, Michaël, Sokolow, Youri, Alexiou, Jean   +3 more
openaire   +4 more sources

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Camurati-Engelmann Disease: Review of Radioclinical Features

Acta Radiologica, 2003
Purpose: To present a retrospective overview of the clinical and radiological features of Camurati-Engelmann disease (CED) in a large family with genetically proven CED. Material and Methods: Clinical features and imaging studies were available in 8 affected patients out of a large Jewish-Iraqi family with 21 affected members in four ...
F M Vanhoenacker, Ruth Gershoni-Baruch, R Brik   +2 more
exaly   +4 more sources

Camurati–Engelmann Disease With Metaphyseal Involvement

European Journal of Radiology Extra, 2004
Abstract Camurati–Engelmann disease (CED) is a rare diaphyseal dysplasia characterized by progressive cortical sclerosis, both internal and external, of diaphysis of long and short tubular bones and sclerosis of base of skull. We report a case of progressive diaphyseal dysplasia with metaphyseal involvement in a 12-year-old female child, who ...
Ravinder Goswami
exaly   +2 more sources

Positive Effects of an Angiotensin II Type 1 Receptor Antagonist in Camurati–Engelmann Disease: A Single Case Observation

American Journal of Medical Genetics, Part A, 2014
Camurati-Engelmann disease is characterized by hyperostosis of the long bones and the skull, muscle atrophy, severe limb pain, and progressive joint contractures in some patients.
Koray Boduroglu, Eda Utine, Pelin Ö Şimşek-Kiper   +2 more
exaly   +2 more sources

Camurati-Engelmann Disease

Reumatología Clínica (English Edition), 2017
1Senior Registrar, Endocrinology, 2Consultant Endocrinologist, 3Consultant Radiologist, 4Senior Registrar, Orthopedic, 5Consultant Orthopedic Surgeon, 6Consultant Histo Pathologist, National Hospital of Sri Lanka. Figure 1. Xray skull – lateral. Figure 2.
Álvaro, de Bonilla Damiá, Francisco Javier, García Gómez   +1 more
openaire   +2 more sources

Bone Scan in Camurati-Engelmann Disease

Clinical Nuclear Medicine, 1998
An entire family was referred to our department to be tested for Camurati-Engelmann disease (progressive diaphyseal dysplasia) because their father had the disorder. Three out of five of his children showed signs of the disorder, with a typical pattern on bone scintigraphy.
S, Vidal-Sicart, F, Pons, N, Guañabens, R, Herranz   +3 more
openaire   +2 more sources