These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 28697927)

  • 21. Facioscapulohumeral muscular dystrophy can be a cause of isolated childhood cognitive dysfunction.
    Hobson-Webb LD; Caress JB
    J Child Neurol; 2006 Mar; 21(3):252-3. PubMed ID: 16901430
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Facio-scapulo-humeral muscular dystrophy with early joint contractures and rigid spine.
    Papadopoulos C; Zouvelou V; Papadimas GK
    Acta Myol; 2019 Mar; 38(1):25-28. PubMed ID: 31309179
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Severe fascioscapulohumeral muscular dystrophy presenting with Coats' disease and mental retardation.
    Bindoff LA; Mjellem N; Sommerfelt K; Krossnes BK; Roberts F; Krohn J; Tranheim RS; Haggerty ID
    Neuromuscul Disord; 2006 Oct; 16(9-10):559-63. PubMed ID: 16935506
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Early onset facioscapulohumeral muscular dystrophy - Long-term follow-up of a patient with total facial diplegia.
    Rudnik-Schöneborn S; Huemer M; Weis J; Sauer E; Meng G
    Neuromuscul Disord; 2019 Dec; 29(12):973-976. PubMed ID: 31708336
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural feature.
    Neudecker S; Krasnianski M; Bahn E; Zierz S
    Acta Neuropathol; 2004 Sep; 108(3):257-9. PubMed ID: 15221332
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical features.
    Dorobek M; van der Maarel SM; Lemmers RJ; Ryniewicz B; Kabzińska D; Frants RR; Gawel M; Walecki J; Hausmanowa-Petrusewicz I
    J Child Neurol; 2015 Apr; 30(5):580-7. PubMed ID: 24717985
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Facioscapulohumeral muscular dystrophy: Report of seven patients].
    Cea G; Jiménez D
    Rev Med Chil; 2015 Mar; 143(3):304-9. PubMed ID: 26005816
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Bilateral Coats' response in a female patient leads to diagnosis of facioscapulohumeral muscular dystrophy.
    Bass SJ; Sherman J; Giovinazzo V
    Optometry; 2011 Feb; 82(2):72-6. PubMed ID: 21130700
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Subclinical facioscapulohumeral muscular dystrophy masquerading as bilateral Coats disease in a woman.
    Vance SK; Wald KJ; Sherman J; Freund KB
    Arch Ophthalmol; 2011 Jun; 129(6):807-9. PubMed ID: 21670353
    [No Abstract]   [Full Text] [Related]  

  • 30. Severe obstructive hypertrophic cardiomyopathy occurring secondary to mitochondrial disease.
    Izgi C; Cevik C; Bakal RB; Ozkan M
    Turk Kardiyol Dern Ars; 2009 Jul; 37(5):332-6. PubMed ID: 19875907
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Significance of Beevor's sign in facioscapulohumeral dystrophy and other neuromuscular diseases.
    Shahrizaila N; Wills AJ
    J Neurol Neurosurg Psychiatry; 2005 Jun; 76(6):869-70. PubMed ID: 15897515
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cardiac amyloidosis presenting as pseudo-hypertrophic cardiomyopathy.
    Papachan A; Sliwa K; Gildenhuys A; Essop R
    Cardiovasc J S Afr; 2004; 15(3):136-8. PubMed ID: 15258625
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Facioscapulohumeral muscular dystrophy presenting as shoulder pain in a baseball player.
    Kaar S; Hazard D; Miller BS
    Arthroscopy; 2005 Sep; 21(9):1145. PubMed ID: 16171643
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
    Deak KL; Lemmers RJ; Stajich JM; Klooster R; Tawil R; Frants RR; Speer MC; van der Maarel SM; Gilbert JR
    Neurology; 2007 Feb; 68(8):578-82. PubMed ID: 17229919
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Facioscapulohumeral muscular dystrophy.
    Padberg GW; van Engelen BG
    Curr Opin Neurol; 2009 Oct; 22(5):539-42. PubMed ID: 19724227
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Alveolar hypoventilation as an early symptom of muscle weakness in facioscapulohumeral muscular dystrophy.
    Rupprecht S; Hagemann G; Witte OW; Schwab M
    Sleep Med; 2009 May; 10(5):592-3. PubMed ID: 18753002
    [No Abstract]   [Full Text] [Related]  

  • 37. [Facioscapulohumeral muscular dystrophy. The spectrum of clinical manifestations and molecular genetic changes].
    Krasnianski M; Neudecker S; Eger K; Schulte-Mattler W; Zierz S
    Nervenarzt; 2003 Feb; 74(2):151-8. PubMed ID: 12596016
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Patient page. Exercise is safe and beneficial for people with facioscapulohumeral muscular dystrophy.
    Brey RL
    Neurology; 2005 Mar; 64(6):E22. PubMed ID: 15781802
    [No Abstract]   [Full Text] [Related]  

  • 39. Prenatal diagnosis for facioscapulohumeral muscular dystrophy (FSHD).
    Upadhyaya M; MacDonald M; Ravine D
    Prenat Diagn; 1999 Oct; 19(10):959-65. PubMed ID: 10521823
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Dysphagia in facioscapulohumeral muscular dystrophy.
    Wohlgemuth M; de Swart BJ; Kalf JG; Joosten FB; Van der Vliet AM; Padberg GW
    Neurology; 2006 Jun; 66(12):1926-8. PubMed ID: 16801662
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.