Category:Media from Orphanet Journal of Rare Diseases

Media in category "Media from Orphanet Journal of Rare Diseases"

The following 102 files are in this category, out of 102 total.

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  1750-1172-1-51-2-l.jpg 589 × 610; 68 KB
  
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  A amelogenesis imperfecta.jpg 360 × 260; 20 KB
  
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  Acromegaly growth hormone levels.JPEG 810 × 319; 40 KB
  
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  Acromegaly hands.JPEG 331 × 232; 17 KB
  
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  Acromegaly pituitary macroadenoma.JPEG 905 × 452; 89 KB
  
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  Acromegaly prognathism.JPEG 401 × 300; 25 KB
  
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  Acromegaly treatment diagram (hy).png 2,489 × 1,620; 859 KB
  
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  Acromegaly treatment diagram.JPEG 917 × 635; 100 KB
  
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  Acute photosensitivity reaction in EPP.jpg 1,200 × 807; 245 KB
  
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  Alpha 1-antitrypsine deficiency lung CT scan.JPEG 641 × 384; 47 KB
  
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  Alpha-1-antitripsin deficiency1.jpg 685 × 497; 65 KB
  
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  Alpha-1-antitripsin deficiency2.jpg 687 × 495; 121 KB
  
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  Alpha-mannosidosis electron micrograph.JPEG 839 × 439; 76 KB
  
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  Alpha-mannosidosis.JPEG 879 × 597; 97 KB
  
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  Alström syndrome.jpg 1,200 × 807; 126 KB
  
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  Angiokeratoma 01.jpg 1,200 × 900; 162 KB
  
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  Arrhythmogenic right ventricular cardiomyopathy - histology.jpg 398 × 471; 87 KB
  
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  Arrhythmogenic right ventricular cardiomyopathy.jpg 315 × 429; 29 KB
  
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  Arvd SEM.jpg 598 × 285; 70 KB
  
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  Arvdd.jpg 635 × 430; 53 KB
  
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  Arvde.jpg 606 × 380; 76 KB
  
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  Atrezja op.jpg 435 × 333; 34 KB
  
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  Atrezja.jpg 607 × 250; 45 KB
  
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  B amelogenesis imperfecta.jpg 360 × 260; 23 KB
  
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  C amelogenesis imperfecta.jpg 360 × 260; 21 KB
  
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  CAVC.jpg 320 × 240; 22 KB
  
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  CAVC.png 500 × 376; 177 KB
  
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  Centronuclear myotubular myopathy.JPEG 720 × 540; 120 KB
  
• Characterization-of-a-distinct-lethal-arteriopathy-syndrome-in-twenty-two-infantsassociated-with-an-1750-1172-7-61-S1.ogv 24 s, 640 × 480; 7.3 MB
  
• Characterization-of-a-distinct-lethal-arteriopathy-syndrome-in-twenty-two-infantsassociated-with-an-1750-1172-7-61-S2.ogv 1.0 s, 800 × 600; 512 KB
  
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  Charge.jpg 1,200 × 1,375; 357 KB
  
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  Child wearing early Cochlear Limited body-worn processor.jpg 739 × 797; 172 KB
  
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  Congenital hereditary endothelial dystrophy 1.JPEG 501 × 500; 81 KB
  
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  Congenital hypertrophy of the retinal pigment epithelium.jpg 709 × 487; 31 KB
  
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  Congenital stromal corneal dystrophy.jpg 800 × 533; 26 KB
  
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  Congenital stromal corneal dystrophy.TIFF 800 × 533; 434 KB
  
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  Congenital stromal dystrophy 2.jpg 800 × 630; 207 KB
  
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  Craniopharyngioma1.jpg 988 × 1,133; 177 KB
  
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  Craniopharyngioma2.jpg 1,200 × 1,777; 261 KB
  
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  Cutaneous histological features of EPP.jpg 1,200 × 820; 293 KB
  
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  D amelogenesis imperfecta.jpg 360 × 260; 19 KB
  
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  DuPanSyndrome1.JPG 399 × 256; 9 KB
  
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  Ellis-vancreveld.jpg 300 × 828; 49 KB
  
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  Fleck dystrophy 1.JPEG 720 × 540; 28 KB
  
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  Fundus of patient with retinitis pigmentosa, early stage.jpg 1,200 × 799; 95 KB
  
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  Fundus of patient with retinitis pigmentosa, end stage.jpg 1,200 × 799; 162 KB
  
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  Fundus of patient with retinitis pigmentosa, mid stage.jpg 871 × 747; 107 KB
  
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  Fundus retinoblastoma.jpg 276 × 229; 15 KB
  
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  G amelogenesis imperfecta.jpg 360 × 260; 20 KB
  
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  Gitelman syndrome.jpg 656 × 650; 74 KB
  
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  Granular corneal dystrophy type II slit lamp.JPEG 1,536 × 1,024; 743 KB
  
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  Greig syndrome 3.JPG 546 × 523; 36 KB
  
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  Greig syndrome.JPG 526 × 522; 18 KB
  
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  Greig syndrome2.JPG 520 × 523; 20 KB
  
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  H amelogenesis imperfecta.jpg 360 × 260; 19 KB
  
• Haploinsufficiency-of-two-histone-modifier-genes-on-6p22.3-ATXN1-and-JARID2-is-associated-with-1750-1172-8-3-S2.ogv 35 s, 960 × 540; 12.74 MB
  
• Haploinsufficiency-of-two-histone-modifier-genes-on-6p22.3-ATXN1-and-JARID2-is-associated-with-1750-1172-8-3-S3.ogv 35 s, 320 × 240; 3.97 MB
  
• Haploinsufficiency-of-two-histone-modifier-genes-on-6p22.3-ATXN1-and-JARID2-is-associated-with-1750-1172-8-3-S4.ogv 1 min 7 s, 960 × 540; 24.58 MB
  
• Haploinsufficiency-of-two-histone-modifier-genes-on-6p22.3-ATXN1-and-JARID2-is-associated-with-1750-1172-8-3-S5.ogv 35 s, 320 × 240; 3.97 MB
  
• Haploinsufficiency-of-two-histone-modifier-genes-on-6p22.3-ATXN1-and-JARID2-is-associated-with-1750-1172-8-3-S6.ogv 1 min 7 s, 960 × 540; 24.58 MB
  
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  Harboyan.JPG 464 × 277; 14 KB
  
• Intra-Erythrocyte-Infusion-of-Dexamethasone-Reduces-Neurological-Symptoms-in-Ataxia-Teleangiectasia-1750-1172-9-5-S4.ogv 2 min 0 s, 720 × 574; 9.12 MB
  
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  Kbg.jpg 285 × 381; 36 KB
  
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  Kbg2.jpg 1,200 × 626; 170 KB
  
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  Kyphoscoliosis hereditary sensory autonomic neuropathy III.jpg 833 × 751; 85 KB
  
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  Lujan.jpg 441 × 683; 68 KB
  
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  Meesmann corneal dystrophy - Multiple opaque spots in the corneal epithelium.JPEG 500 × 500; 60 KB
  
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  Morbus Fabry EKG 01.jpg 1,200 × 1,816; 499 KB
  
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  Morbus Fabry kidney biopsy 02.jpg 1,200 × 911; 392 KB
  
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  Mouth ECS.jpg 531 × 822; 92 KB
  
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  Mowat-Wilson-2.JPEG 378 × 786; 66 KB
  
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  Mowat-Wilson.JPEG 374 × 1,078; 102 KB
  
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  Naxos disease.jpg 1,200 × 728; 216 KB
  
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  Ollier radio.jpg 885 × 424; 35 KB
  
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  Ollier radio2.jpg 561 × 777; 49 KB
  
• Phenotypical-variation-within-22-families-with-Pompe-disease-1750-1172-8-182-S1.ogv 54 s, 640 × 480; 7.55 MB
  
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  Polydactyly ECS.jpg 755 × 495; 72 KB
  
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  Pontocerebellar hypoplasia MRI 1750-1172-7-18-4-l.jpg 1,200 × 1,698; 347 KB
  
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  Posterior polymorphous corneal dystrophy 1.JPEG 500 × 323; 94 KB
  
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  Pouch atresia.jpg 279 × 466; 25 KB
  
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  Primary intestinal lymphangiectasia (Waldmann's disease) - legs.jpg 1,173 × 1,488; 521 KB
  
• Quantitative-analysis-of-ciliary-beating-in-primary-ciliary-dyskinesia-a-pilot-study-1750-1172-7-78-S1.ogv 10 s, 256 × 192; 2.04 MB
  
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  Reis-Bücklers corneal dystrophy. Reticular opacity in the superficial cornea.JPEG 500 × 500; 64 KB
  
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  Rhabdomyoma.jpg 410 × 370; 24 KB
  
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  Robinow syndrome.jpg 1,200 × 762; 185 KB
  
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  Robinow syndrome2.jpg 1,200 × 796; 132 KB
  
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  Skeletal defects in patient with KBG syndrome.jpg 1,200 × 901; 203 KB
  
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  Subepithelial mucinous corneal dystrophy 1.JPEG 1,100 × 742; 443 KB
  
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  Sweet-syndrome skin.png 1,337 × 586; 574 KB
  
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  Temtamy.jpg 1,200 × 801; 161 KB
  
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  THE syndrome (4).jpg 416 × 310; 24 KB
  
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  THE syndrome (5).jpg 397 × 293; 23 KB
  
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  THE syndrome (6).jpg 299 × 386; 30 KB
  
• The-c.429 452-duplication-of-the-ARX-gene-a-unique-developmental-model-of-limb-kinetic-apraxia-1750-1172-9-25-S5.ogv 4.4 s, 640 × 480; 1.58 MB
  
• The-c.429 452-duplication-of-the-ARX-gene-a-unique-developmental-model-of-limb-kinetic-apraxia-1750-1172-9-25-S6.ogv 19 s, 640 × 480; 5.94 MB
  
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  Transposition great arteries Orphanet 1750-1172-3-27-1.JPEG 626 × 515; 32 KB
  
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  Transposition great arteries Orphanet 1750-1172-3-27-2.JPEG 633 × 523; 33 KB
  
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  Transposition great arteries Orphanet 1750-1172-3-27-4.JPEG 616 × 516; 32 KB
  
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  Tricho-hepato-enteric syndrome (1).jpg 444 × 483; 35 KB
  
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  Tricho-hepato-enteric syndrome (3).jpg 691 × 478; 134 KB
  
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  Tricho-hepato-enteric syndrome.jpg 318 × 474; 33 KB
  
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  Trilateral retinoblastoma.jpg 192 × 201; 11 KB