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 *

96 related articles for article (PubMed ID: 7801048)

  • 1. [Familial deficiency of C7 associated with adrenomyeloneuropathy].
    Pelletier J; Pestre P; ali Chérif A; Drancourt M; Gallais H; Khalil R
    Rev Neurol (Paris); 1994; 150(1):78-80. PubMed ID: 7801048
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A variant of adrenomyeloneuropathy in a family with adrenoleukodystrophy and adrenomyeloneuropathy.
    Simpson DA; Pawlak AM; Nigro MA; Wishnow R
    J Am Osteopath Assoc; 1994 Sep; 94(9):745-8, 751-2. PubMed ID: 7995738
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Familial deficiency of complement factor 7: association with bacterial meningitis. Apropos of 3 recent cases].
    Drancourt M; Raoult D; Lesavre P; Gallais H; Casanova P
    Pathol Biol (Paris); 1988 Jun; 36(6):825-8. PubMed ID: 3047643
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Recurrent Neisseria meningitidis meningitis associated with homozygote complement C7 fraction deficiency].
    Angibaud G; Durand G; Rascol A; Clanet M
    Rev Neurol (Paris); 1992; 148(3):237-8. PubMed ID: 1604143
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Apropos of a familial case of adrenoleukodystrophy related to X chromosome diagnosed prenatally].
    Parent P; Le Meur F; Alix D; Le Fur JM; Toudic L; Castel Y
    Pediatrie; 1987; 42(4):297-301. PubMed ID: 3671029
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Combined-heterozygous deficiency of complement C7 in a patient with recurrent meningitis].
    Schirinzi R; Lantin JP; Frémeaux-Bacchi V; Schifferli JA; Trendelenburg M
    Med Klin (Munich); 2006 Aug; 101(8):655-8. PubMed ID: 16896572
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Meningococcal meningitis in isolated familial deficiency of the 7th complement component, C7].
    Straub PW; Späth P
    Schweiz Med Wochenschr; 1986 May; 116(21):699-702. PubMed ID: 3726502
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Adrenoleukomyeloneuropathy. A familial case].
    Gastaut JL; Pellissier JF; Pfister B; Figarella-Branger D; Michel B
    Rev Neurol (Paris); 1988; 144(5):338-46. PubMed ID: 3420352
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Examination of very long chain fatty acids in diagnosis of x-linked adrenoleukodystrophy].
    Stradomska TJ; Tylki-Szymańska A
    Pediatr Pol; 1996 Mar; 71(3):197-201. PubMed ID: 8966090
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Backache as the initial symptom of adrenomyeloneuropathy].
    Benito-León J; Zamorano T; Martín-Peña G; Tapia MA; Alvarez-Linera J
    Rev Neurol; 2000 Dec 16-31; 31(12):1167-70. PubMed ID: 11205553
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Complement C7 deficiency presenting as recurrent aseptic meningitis.
    Corvini M; Randolph C; Aronin SI
    Ann Allergy Asthma Immunol; 2004 Aug; 93(2):200-5. PubMed ID: 15328683
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multislice proton magnetic resonance spectroscopic imaging in X-linked adrenoleukodystrophy.
    Kruse B; Barker PB; van Zijl PC; Duyn JH; Moonen CT; Moser HW
    Ann Neurol; 1994 Oct; 36(4):595-608. PubMed ID: 7944292
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes.
    Berger J; Molzer B; Faé I; Bernheimer H
    Biochem Biophys Res Commun; 1994 Dec; 205(3):1638-43. PubMed ID: 7811247
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Adrenomyeloneuropathy--an unusual X chromosome-linked disease].
    Holmberg BH; Hägg E
    Lakartidningen; 1990 Nov; 87(46):3873-4. PubMed ID: 2233068
    [No Abstract]   [Full Text] [Related]  

  • 16. Adrenomyeloneuropathy and hypothyroidism. A 15 year follow-up case report.
    Laureti S; Lucarelli M; Santeusanio F; Casucci G
    Recenti Prog Med; 1992 Feb; 83(2):67-72. PubMed ID: 1502421
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Adrenomyeloneuropathy.
    Dickey W; Lyttle JA; Sawhney BB; Kennedy L
    Ulster Med J; 1987 Oct; 56(2):149-51. PubMed ID: 3445395
    [No Abstract]   [Full Text] [Related]  

  • 18. [Adrenomyeloneuropathy as a cause of Addison's disease].
    Baerwald C; Ehlenz K; Körber R; Hillig U; von Wichert P
    Dtsch Med Wochenschr; 1991 Feb; 116(7):254-8. PubMed ID: 1993440
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial late complement component (C6, C7) deficiency with chronic meningococcemia.
    Clough JD; Clough ML; Weinstein A; Calabrese LH; Mansfield LR; Gulick P; Gavan T; Braun WE
    Arch Intern Med; 1980 Jul; 140(7):929-33. PubMed ID: 7387302
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Combined familial C7 and C4B deficiency in an adult with meningococcal disease.
    Chapel HM; Peto TE; Luzzi GA; Thompson RA; Fielder AH; Batchelor JR
    Clin Exp Immunol; 1987 Jan; 67(1):55-8. PubMed ID: 3497744
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.