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 *

143 related articles for article (PubMed ID: 31253576)

  • 41. Low rate of production of apolipoproteins B100 and AI in 2 patients with Anderson disease (chylomicron retention disease).
    Ouguerram K; Zaïr Y; Kasbi-Chadli F; Nazih H; Bligny D; Schmitz J; Aparicio T; Chétiveaux M; Magot T; Aggerbeck LP; Samson-Bouma ME; Krempf M
    Arterioscler Thromb Vasc Biol; 2012 Jun; 32(6):1520-5. PubMed ID: 22441101
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Fat accumulation in enterocytes: a key to the diagnosis of abetalipoproteinemia or homozygous hypobetalipoproteinemia.
    Desomer L; De Vos M; De Looze D
    Endoscopy; 2015; 47 Suppl 1 UCTN():E223-4. PubMed ID: 26062159
    [No Abstract]   [Full Text] [Related]  

  • 43. Studying lipoprotein trafficking in zebrafish, the case of chylomicron retention disease.
    Schlegel A
    J Mol Med (Berl); 2015 Feb; 93(2):115-8. PubMed ID: 25572701
    [No Abstract]   [Full Text] [Related]  

  • 44. Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia.
    Di Filippo M; Moulin P; Roy P; Samson-Bouma ME; Collardeau-Frachon S; Chebel-Dumont S; Peretti N; Dumortier J; Zoulim F; Fontanges T; Parini R; Rigoldi M; Furlan F; Mancini G; Bonnefont-Rousselot D; Bruckert E; Schmitz J; Scoazec JY; Charrière S; Villar-Fimbel S; Gottrand F; Dubern B; Doummar D; Joly F; Liard-Meillon ME; Lachaux A; Sassolas A
    J Hepatol; 2014 Oct; 61(4):891-902. PubMed ID: 24842304
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Current Diagnosis and Management of Familial Hypobetalipoproteinemia 1.
    Wakabayashi T; Takahashi M; Okazaki H; Okazaki S; Yokote K; Tada H; Ogura M; Ishigaki Y; Yamashita S; Harada-Shiba M;
    J Atheroscler Thromb; 2024 Jul; 31(7):1005-1023. PubMed ID: 38710625
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Guidance for the diagnosis and treatment of hypolipidemia disorders.
    Bredefeld C; Hussain MM; Averna M; Black DD; Brin MF; Burnett JR; Charrière S; Cuerq C; Davidson NO; Deckelbaum RJ; Goldberg IJ; Granot E; Hegele RA; Ishibashi S; Karmally W; Levy E; Moulin P; Okazaki H; Poinsot P; Rader DJ; Takahashi M; Tarugi P; Traber MG; Di Filippo M; Peretti N
    J Clin Lipidol; 2022; 16(6):797-812. PubMed ID: 36243606
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Chylomicron retention disease: report of two cases from a Greek Island.
    Papadogeorgou P; Roma E; Sassolas A; Orfanou I; Malliarou A; Sakka S; Chouliaras G
    J Pediatr Endocrinol Metab; 2012; 25(11-12):1191-4. PubMed ID: 23329770
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Comparison of two polygenic risk scores to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects.
    Cefalù AB; Spina R; Noto D; Rabacchi C; Giammanco A; Simone ML; Brucato F; Scrimali C; Gueli-Alletti MG; Barbagallo CM; Tarugi P; Averna MR
    J Clin Lipidol; 2022; 16(4):530-537. PubMed ID: 35589500
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Molecular characterization of Tunisian families with abetalipoproteinemia and identification of a novel mutation in MTTP gene.
    Najah M; Youssef SM; Yahia HM; Afef S; Awatef J; Saber H; Fadhel NM; Sassolas A; Naceur SM
    Diagn Pathol; 2013 Apr; 8():54. PubMed ID: 23556456
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities.
    Silvain M; Bligny D; Aparicio T; Laforêt P; Grodet A; Peretti N; Ménard D; Djouadi F; Jardel C; Bégué JM; Walker F; Schmitz J; Lachaux A; Aggerbeck LP; Samson-Bouma ME
    Clin Genet; 2008 Dec; 74(6):546-52. PubMed ID: 18786134
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Homozygous hypobetalipoproteinemia with spared chylomicron formation.
    Harano Y; Kojima H; Nakano T; Harada M; Kashiwagi A; Nakajima Y; Hidaka TH; Ohtsuki T; Suzuki T; Tamura A
    Metabolism; 1989 Jan; 38(1):1-7. PubMed ID: 2909827
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Functional overlap between the mammalian
    Tang VT; Xiang J; Chen Z; McCormick J; Abbineni PS; Chen XW; Hoenerhoff M; Emmer BT; Khoriaty R; Lin JD; Ginsburg D
    Proc Natl Acad Sci U S A; 2024 May; 121(19):e2322164121. PubMed ID: 38687799
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A truncated species of apolipoprotein B (B-38.7) in a patient with homozygous hypobetalipoproteinemia associated with diabetes mellitus.
    Ohashi K; Ishibashi S; Yamamoto M; Osuga J; Yazaki Y; Yukawa S; Yamada N
    Arterioscler Thromb Vasc Biol; 1998 Aug; 18(8):1330-4. PubMed ID: 9714141
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Homozygous familial hypobetalipoproteinemia. Increased LDL catabolism in hypobetalipoproteinemia due to a truncated apolipoprotein B species, apo B-87Padova.
    Gabelli C; Bilato C; Martini S; Tennyson GE; Zech LA; Corsini A; Albanese M; Brewer HB; Crepaldi G; Baggio G
    Arterioscler Thromb Vasc Biol; 1996 Sep; 16(9):1189-96. PubMed ID: 8792774
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Chylomicron Retention Disease in A Male Infant: A Rare Case from Pakistan.
    Kumar S; Nanjiani D; Tahir F; Azim D; Parkash O
    Cureus; 2020 Mar; 12(3):e7184. PubMed ID: 32257723
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Lipids Responsible for Intestinal or Hepatic Disorder: When to Suspect a Familial Intestinal Hypocholesterolemia?
    Sissaoui S; Cochet M; Poinsot P; Bordat C; Collardeau-Frachon S; Lachaux A; Lacaille F; Peretti N
    J Pediatr Gastroenterol Nutr; 2021 Jul; 73(1):4-8. PubMed ID: 33853111
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia.
    Di Leo E; Lancellotti S; Penacchioni JY; Cefalù AB; Averna M; Pisciotta L; Bertolini S; Calandra S; Gabelli C; Tarugi P
    Atherosclerosis; 2005 Jun; 180(2):311-8. PubMed ID: 15910857
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The hypobetalipoproteinemias.
    Schonfeld G
    Annu Rev Nutr; 1995; 15():23-34. PubMed ID: 8527219
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Malabsorption, hypocholesterolemia, and fat-filled enterocytes with increased intestinal apoprotein B. Chylomicron retention disease.
    Roy CC; Levy E; Green PH; Sniderman A; Letarte J; Buts JP; Orquin J; Brochu P; Weber AM; Morin CL; Marcel Y; Deckelbaum RJ
    Gastroenterology; 1987 Feb; 92(2):390-9. PubMed ID: 3792776
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Chylomicron retention disease: a rare aetiology of failure to thrive.
    Sunkoj Y; Yu Z; Altaf A; Talathi S
    BMJ Case Rep; 2024 May; 17(5):. PubMed ID: 38749523
    [TBL] [Abstract][Full Text] [Related]  

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