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 *

140 related articles for article (PubMed ID: 19664540)

  • 1. Manifestation of neurofibromatosis 1 in a patient with X-linked adrenoleukodystrophy.
    Yamada H; Izumi T
    Pediatr Neurol; 2009 Sep; 41(3):211-4. PubMed ID: 19664540
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.
    Charrow J; Listernick R; Ward K
    Am J Med Genet; 1993 Mar; 45(5):606-8. PubMed ID: 8456833
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Early changes in magnetic resonance tomography in adrenoleukomyeloneuropathy].
    Otto V; Reilmann L
    Nervenarzt; 1994 Apr; 65(4):264-6. PubMed ID: 8015634
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Pigmentation (café au lait spots), 2) family history].
    Kobayashi K; Takashima S
    No To Shinkei; 1996 Aug; 48(8):762. PubMed ID: 8797212
    [No Abstract]   [Full Text] [Related]  

  • 5. [Symptomatic heterozygotic adrenoleukodystrophy in adults. 10 cases].
    Ménage P; Carreau V; Tourbah A; Fontaine B; Paturneau-Jouas M; Gout O; Lubetzki C; Baumann N; Lyon-Caen O
    Rev Neurol (Paris); 1993; 149(8-9):445-54. PubMed ID: 8009141
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Frontal pseudo-tumoral form of adrenoleukodystrophy].
    Koussa S; Megarbane A; Rizk T; Tamraz J; Chemaly R
    Rev Neurol (Paris); 2000 Nov; 156(11):1017-9. PubMed ID: 11119055
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [The case of neurofibromatosis type ! in a 5-year-old boy].
    Przybysz K; Nowak K; Kobielski A; Bolanowski W; Bodalski J
    Wiad Lek; 1998; 51 Suppl 4():334-7. PubMed ID: 10731995
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An index case of adrenomyeloneuropathy in a Chinese man.
    Ong BK; Lee KO; Lee T; Chong PN
    Singapore Med J; 1994 Dec; 35(6):643-5. PubMed ID: 7761896
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Café au lait spots without giant pigment granules. Occurrence in suspected neurofibromatosis.
    Silvers DN; Greenwood RS; Helwig EB
    Arch Dermatol; 1974 Jul; 110(1):87-8. PubMed ID: 4213778
    [No Abstract]   [Full Text] [Related]  

  • 10. Adrenoleukodystrophy: a correlation between saturated very long-chain fatty acids in mononuclear cells and phenotype.
    Antoku Y; Koike F; Ohtsuka Y; Sakai T; Tsukamoto K; Nagara H; Iwashita H; Goto I
    Ann Neurol; 1991 Jul; 30(1):101-3. PubMed ID: 1929220
    [TBL] [Abstract][Full Text] [Related]  

  • 11. X-linked adrenoleukodystrophy. The Saudi experience.
    Al-Essa MA; Sakati NA; Bakheet SM; Patay ZJ; Dabbagh O; Chaves-Carbello E; Ozand PT
    Saudi Med J; 2000 Jan; 21(1):61-71. PubMed ID: 11533753
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Radiology case of the month. Café-au-lait spots. Neurofibromatosis type 1.
    Gupta A; Neitzschman HR; Schroder M
    J La State Med Soc; 2002; 154(5):221-2. PubMed ID: 12440746
    [No Abstract]   [Full Text] [Related]  

  • 13. Coma as an acute presentation of adrenoleukodystrophy.
    Ravid S; Diamond AS; Eviatar L
    Pediatr Neurol; 2000 Mar; 22(3):237-9. PubMed ID: 10734258
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Central nervous system malformations and white matter changes in pseudo-neonatal adrenoleukodystrophy.
    Kyllerman M; Blomstrand S; Månsson JE; Conradi NG; Hindmarsh T
    Neuropediatrics; 1990 Nov; 21(4):199-201. PubMed ID: 2290480
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [X-linked adrenoleukodystrophy. A case report].
    Mingorance Delgado A; Tabernero Pérez C; Tapia Muñoz J; Martín Aguado MJ; Lloret Sempere T; Flores Serrano J
    An Esp Pediatr; 1999 May; 50(5):509-12. PubMed ID: 10394195
    [No Abstract]   [Full Text] [Related]  

  • 16. [Cerebral adrenomyeloneuropathy as a late type of adrenoleukodystrophy: case report].
    Siger-Zajdel M; Stradomska TJ; Rozniecki J; Zielińska M; Selmaj K
    Neurol Neurochir Pol; 2000; 34(3):579-85. PubMed ID: 10979550
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Simvastatin and plasma very-long-chain fatty acids in X-linked adrenoleukodystrophy.
    Verrips A; Willemsen MA; Rubio-Gozalbo E; De Jong J; Smeitink JA
    Ann Neurol; 2000 Apr; 47(4):552-3. PubMed ID: 10762175
    [No Abstract]   [Full Text] [Related]  

  • 18. The myth of six café-au-lait spots in the peripheral form of neurofibromatosis.
    Goodman RM; Tiron A; Katznelson AB; Zehavi C; Romano A; Levine G
    Neurofibromatosis; 1988; 1(1):54. PubMed ID: 3152529
    [No Abstract]   [Full Text] [Related]  

  • 19. Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids.
    Brown FR; McAdams AJ; Cummins JW; Konkol R; Singh I; Moser AB; Moser HW
    Johns Hopkins Med J; 1982 Dec; 151(6):344-51. PubMed ID: 7176294
    [No Abstract]   [Full Text] [Related]  

  • 20. Allogeneic bone marrow transplantation in adrenoleukodystrophy: clinical, pathologic, and biochemical studies.
    Yeager AM; Moser HW; Tutschka PJ; Saral R; Moser AE; Kumar AA; Santos GW
    Birth Defects Orig Artic Ser; 1986; 22(1):79-100. PubMed ID: 3516244
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.