BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 30649222)

  • 41. XPR1 mutations are a rare cause of primary familial brain calcification.
    Anheim M; López-Sánchez U; Giovannini D; Richard AC; Touhami J; N'Guyen L; Rudolf G; Thibault-Stoll A; Frebourg T; Hannequin D; Campion D; Battini JL; Sitbon M; Nicolas G
    J Neurol; 2016 Aug; 263(8):1559-64. PubMed ID: 27230854
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Neuropsychological heterogeneity in patients with primary familial brain calcification due to a novel mutation in SLC20A2.
    Chiriaco C; Novellino F; Salsone M; Gagliardi M; Morelli M; Quattrone A
    Neurol Sci; 2018 Feb; 39(2):379-380. PubMed ID: 28936702
    [No Abstract]   [Full Text] [Related]  

  • 43. [Familial strio-pallido++-dentate calcification].
    Prieto JM; Pardellas H; Sobrido MJ; Lema M; Dapena D; Castro A
    Rev Neurol; 1997 Aug; 25(144):1213-5. PubMed ID: 9340152
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Primary familial brain calcification linked to deletion of 5' noncoding region of SLC20A2.
    Pasanen P; Mäkinen J; Myllykangas L; Guerreiro R; Bras J; Valori M; Viitanen M; Baumann M; Tienari PJ; Pöyhönen M; Baumann P
    Acta Neurol Scand; 2017 Jul; 136(1):59-63. PubMed ID: 27726124
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease.
    Reardon W; Hockey A; Silberstein P; Kendall B; Farag TI; Swash M; Stevenson R; Baraitser M
    Am J Med Genet; 1994 Aug; 52(1):58-65. PubMed ID: 7977464
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Lenticulodentate calcification.
    Hastings-James R
    Radiology; 1970 Dec; 97(3):571-6. PubMed ID: 5491742
    [No Abstract]   [Full Text] [Related]  

  • 47. [Familial idiopathic striato-pallido-dentate calcifications: clinical and brain imaging study in a family].
    Le Ber I; Marié RM; Lalevée C; Chabot B; Allouche S; Defer GL
    Rev Neurol (Paris); 2003 Jan; 159(1):43-9. PubMed ID: 12618652
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Primary familial brain calcification: Genetic analysis and clinical spectrum.
    Taglia I; Mignarri A; Olgiati S; Menci E; Petrocelli PL; Breedveld GJ; Scaglione C; Martinelli P; Federico A; Bonifati V; Dotti MT
    Mov Disord; 2014 Nov; 29(13):1691-5. PubMed ID: 25284758
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Primary brain calcification in patients undergoing treatment with the biphosphanate alendronate.
    Oliveira JR; Oliveira MF
    Sci Rep; 2016 Mar; 6():22961. PubMed ID: 26976513
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Two siblings with microcephaly associated with calcification of cerebral white matter.
    Ishitsu T; Chikazawa S; Matsuda I
    Jinrui Idengaku Zasshi; 1985 Sep; 30(3):213-7. PubMed ID: 3834201
    [No Abstract]   [Full Text] [Related]  

  • 51. Phosphate Transporters Expression in Patients with Primary Familial Brain Calcifications.
    Pimentel LF; Lemos RR; Oliveira JR
    J Mol Neurosci; 2017 Aug; 62(3-4):276-280. PubMed ID: 28578517
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Recessive osteopetrosis with cerebral calcifications. Study of 3 adult subjects in 2 consanguineous families].
    Leone G
    Radiol Med; 1982 May; 68(5):373-8. PubMed ID: 7111790
    [No Abstract]   [Full Text] [Related]  

  • 53. Rare associations with Goldenhar syndrome.
    Vatwani V; Verma N; Palta SC; Dogra BB
    Indian Pediatr; 1994 Jan; 31(1):72-3. PubMed ID: 7883328
    [No Abstract]   [Full Text] [Related]  

  • 54. A PDGFB mutation causes paroxysmal nonkinesigenic dyskinesia with brain calcification.
    Wang C; Ma X; Xu X; Huang B; Sun H; Li L; Zhang M; Liu JY
    Mov Disord; 2017 Jul; 32(7):1104-1106. PubMed ID: 28556368
    [No Abstract]   [Full Text] [Related]  

  • 55. A novel GALNT3 mutation in a pseudoautosomal dominant form of tumoral calcinosis: evidence that the disorder is autosomal recessive.
    Ichikawa S; Lyles KW; Econs MJ
    J Clin Endocrinol Metab; 2005 Apr; 90(4):2420-3. PubMed ID: 15687324
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Primary familial brain calcification with a novel SLC20A2 mutation: Analysis of PiT-2 expression and localization.
    Taglia I; Formichi P; Battisti C; Peppoloni G; Barghigiani M; Tessa A; Federico A
    J Cell Physiol; 2018 Mar; 233(3):2324-2331. PubMed ID: 28722801
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Paroxysmal Kinesigenic Dyskinesia Secondary to Brain Calcification with a Homozygous MYORG Mutation.
    Du J; Zhu X; Liu J; Tan Y
    Mov Disord; 2021 Nov; 36(11):2699-2701. PubMed ID: 34346093
    [No Abstract]   [Full Text] [Related]  

  • 58. Familial idiopathic cerebral calcifications.
    Boller F; Boller M; Gilbert J
    J Neurol Neurosurg Psychiatry; 1977 Mar; 40(3):280-5. PubMed ID: 886353
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Asymptomatic familial basal ganglia calcification with autosomal dominant inheritance: a family report].
    Yamada N; Hayashi T
    No To Hattatsu; 2000 Nov; 32(6):515-9. PubMed ID: 11144166
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A familial syndrome with coats' reaction retinal angiomas, hair and nail defects and intracranial calcification.
    Tolmie JL; Browne BH; McGettrick PM; Stephenson JB
    Eye (Lond); 1988; 2 ( Pt 3)():297-303. PubMed ID: 3402627
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.