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 *

146 related articles for article (PubMed ID: 37331934)

  • 61. Two Italian patients with novel AAAS gene mutation expand allelic and phenotypic spectrum of triple A (Allgrove) syndrome.
    Palka C; Giuliani R; Brancati F; Mohn A; Di Muzio A; Calabrese O; Huebner A; De Grandis D; Chiarelli F; Ferlini A; Stuppia L
    Clin Genet; 2010 Mar; 77(3):298-301. PubMed ID: 20447142
    [No Abstract]   [Full Text] [Related]  

  • 62. Allgrove (Triple A) Syndrome: A Case Report from the Kashmir Valley.
    Misgar RA; Pala NA; Ramzan M; Wani AI; Bashir MI; Laway BA
    Endocrinol Metab (Seoul); 2015 Dec; 30(4):604-6. PubMed ID: 26354489
    [TBL] [Abstract][Full Text] [Related]  

  • 63. The nuclear pore complex protein ALADIN is anchored via NDC1 but not via POM121 and GP210 in the nuclear envelope.
    Kind B; Koehler K; Lorenz M; Huebner A
    Biochem Biophys Res Commun; 2009 Dec; 390(2):205-10. PubMed ID: 19782045
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Allgrove syndrome: case report of 7 years old boy from Bahawalpur.
    Akram S; Khan MA; Rehman A
    J Pak Med Assoc; 2018 Aug; 68(8):1260-1262. PubMed ID: 30108399
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Neurological features in adult Triple-A (Allgrove) syndrome.
    Vallet AE; Verschueren A; Petiot P; Vandenberghe N; Nicolino M; Roman S; Pouget J; Vial C
    J Neurol; 2012 Jan; 259(1):39-46. PubMed ID: 21656342
    [TBL] [Abstract][Full Text] [Related]  

  • 66. AAA Syndrome, Case Report of a Rare Disease.
    Shah SWH; Butt AK; Malik K; Alam A; Shahzad A; Khan AA
    Pak J Med Sci; 2017; 33(6):1512-1516. PubMed ID: 29492088
    [TBL] [Abstract][Full Text] [Related]  

  • 67. The triple "a" syndrome confirmed by molecular analysis: a case report of 7-year-old boy.
    Iwanczak F; Smigiel R; Blitek A; Huebner A
    J Pediatr Gastroenterol Nutr; 2005 Jan; 40(1):87-9. PubMed ID: 15625433
    [No Abstract]   [Full Text] [Related]  

  • 68. Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrima.
    Moore PS; Couch RM; Perry YS; Shuckett EP; Winter JS
    Clin Endocrinol (Oxf); 1991 Feb; 34(2):107-14. PubMed ID: 1850671
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Familial occurrence of adrenocortical insufficiency in two brothers with Allgrove syndrome. A case report of 4A (Allgrove) syndrome with epilepsy and a new AAAS gene mutation.
    Kurca E; Grofik M; Kucera P; Varsik P
    Neuro Endocrinol Lett; 2005 Oct; 26(5):499-502. PubMed ID: 16264411
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome.
    Dumic M; Barišic N; Kusec V; Stingl K; Skegro M; Stanimirovic A; Koehler K; Huebner A
    Eur J Pediatr; 2012 Oct; 171(10):1453-9. PubMed ID: 22538409
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Spectrum of mutations of the AAAS gene in Allgrove syndrome: lack of mutations in six kindreds with isolated resistance to corticotropin.
    Sandrini F; Farmakidis C; Kirschner LS; Wu SM; Tullio-Pelet A; Lyonnet S; Metzger DL; Bourdony CJ; Tiosano D; Chan WY; Stratakis CA
    J Clin Endocrinol Metab; 2001 Nov; 86(11):5433-7. PubMed ID: 11701718
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Changes in differential gene expression in fibroblast cells from patients with triple A syndrome under oxidative stress.
    Koehler K; End K; Kind B; Landgraf D; Mitzscherling P; Huebner A
    Horm Metab Res; 2013 Feb; 45(2):102-8. PubMed ID: 23315990
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Clinical decision making and application of an active rehabilitation program for a person with the neuromuscular symptoms of Allgrove syndrome: a case report.
    Adams JT
    Physiother Theory Pract; 2020 Sep; 36(9):1035-1042. PubMed ID: 30501443
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Familial glucocorticoid deficiency, alacrimia and achalasia--Allgrove syndrome.
    Muranjan MN; Gurav M; Surve T; Deshmukh CT; Bharucha BA
    Indian J Pediatr; 1999; 66(1):151-4. PubMed ID: 10798051
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Mice lacking the nuclear pore complex protein ALADIN show female infertility but fail to develop a phenotype resembling human triple A syndrome.
    Huebner A; Mann P; Rohde E; Kaindl AM; Witt M; Verkade P; Jakubiczka S; Menschikowski M; Stoltenburg-Didinger G; Koehler K
    Mol Cell Biol; 2006 Mar; 26(5):1879-87. PubMed ID: 16479006
    [TBL] [Abstract][Full Text] [Related]  

  • 76. [A case of triple A syndrome with c.463C>T mutation in the AAAS gene].
    Hirosawa H; Konishi H; Nukui T; Hayashi T; Dougu N; Nakatsuji Y
    Rinsho Shinkeigaku; 2022 Sep; 62(9):740-743. PubMed ID: 36031376
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Allgrove syndrome--a syndrome of primary adrenocortical insufficiency with achalasia of the cardia and deficient tear production.
    Bhargavan PV; Kumar KM; Rajendran VR; Fassaludeen AS
    J Assoc Physicians India; 2003 Jul; 51():726-8. PubMed ID: 14621049
    [TBL] [Abstract][Full Text] [Related]  

  • 78. The small, spastic, and furrowed tongue of Allgrove syndrome.
    Houlden H
    Neurology; 2009 Apr; 72(15):1366. PubMed ID: 19365062
    [No Abstract]   [Full Text] [Related]  

  • 79. Allgrove syndrome and motor neuron disease.
    de Freitas MRG; Orsini M; Araújo APQC; João Abraão L; Barbosa GM; França MC; Correia L; Bastos VH; Trajano E; da Sant'Anna M
    Neurol Int; 2018 May; 10(2):7436. PubMed ID: 30069287
    [TBL] [Abstract][Full Text] [Related]  

  • 80. The transmembrane nucleoporin NDC1 is required for targeting of ALADIN to nuclear pore complexes.
    Yamazumi Y; Kamiya A; Nishida A; Nishihara A; Iemura S; Natsume T; Akiyama T
    Biochem Biophys Res Commun; 2009 Nov; 389(1):100-4. PubMed ID: 19703420
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.