PubMed for id: 82769

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38313348,37168645,36898020,35449524,35125723,34946929,34413666,33797866,33488128,33016646,32824233,32327622,31513964,31472034,30937941,30583831,30389309,29907970,29373985,29085829,28363629,28067690,28027403,27896572,27614249,27551308,27252822,26774647,26749401,26621434,25279825,25152992,24872867,24106505,23978024,23780917,23649408,22407746,22297252,21748766,21113736,20858542,20301349,20221534,18421430,17427110,17339196,17264300,17229647,16960153,16424663,15997423,15967692,15811010,15685557,15453783,15315789,15194541,15099344,14982873,14982867,14647275,14630809,12891378,12548385,12528123,12490283,12482411,12469120,12382199,12064925,11778658,10950940,10942934,10772871,10205270,8130638,2856444,2174476,1707654,25150122,17951290,17607352,37119411,36738397,35171259,35149774,34792696,34530087,33559412,32993568,32603552,31286966,30746893,30553600,30362946,29691844,29512696,29230833,29134618,28481424,28007423,27753142,27665106,27518069,26633544,26474245,26238956,26142323,26028554,26027705,25959919,25666510,25588876,25085240,25064704,24321703,24116172,22408404,22367438,21993681,21960693,21901658,21882038,21725613,21626137,21551127,21411349,21193839,21054916,20200618,20044606,19751239,19642734,19571663,19386095,19342478,19318570,19287179,19258504,19252488,19252486,19229506,18827264,18823803,18762941,18491292,18430498,18384687,18287331,18248513,18160816,17949288,17768121,17726683,17593421,17540536,17331953,17245317,17124037,17007103,16982849,16939499,16868025,16604073,16493621,16234038,16160184,16103117,16099526,16075058,15998830,15942838,15875150,15842597,15610558,15603911,15590393,15557369,15528154,15506716,15486069,15315977,15205326,15198949,15147384,15138164,15089902,12663437,12547233,12547231,12060140,11983450,11005792,11001626,10942923,10865496,10802645,10774476,10216143,10088633,9450181,9446792,8835345,7529856,1701409,1651985,38662083,38643663,38620615,38394389,38310100,38145590,38020292,37719963,37603641,37582372,37529719,37455080,37408807,37094045,37057345,36982924,36356177,36278929,36274057,35974196,35780234,35740680,35406401,35339622,34855228,34607725,34359320,34329438,34253291,33946512,33882707,33807929,33341395,33258947,33236024,32808318,32650904,32522605,32473429,32428847,32278388,32258529,32251525,32039031,31928849,31798784,31663628,31518385,31380708,31174104,31124687,31051719,31021524,30865445,30678006,30601004,30499122,30289729,30213871,30129484,30074458,29995332,29688837,29488247,29445730,29396911,29364085,29336081,29332852,29314247,29220535,29199911,29189105,29152553,29115297,28974781,28974780,28715700,28625392,28589951,28588315,28528421,28450157,28407623,28055120,28043096,28006104,27927920,27837028,27821398,27800515,27163957,27110360,27085542,26911319,26889381,26836489,26771219,26685997,26633708,26516623,26435062,26431312,26359661,26286373,26183375,26160012,26159676,26115193,25986058,25938661,25899911,25873621,25865550,25753718,25721938,25702573,25492369,25307625,25036862,24904995,24830674,24677772,24599999,24547685,24533966,24433106,24365099,24307616,24100642,23963250,23916741,23903025,23806388,23780638,23376482,22967209,22730238,22713833,22663300,22447462,22392951,22035764,22005221,21997682,21848322,21841507,21766504,21751245,21689086,21574622,21342386,21254224,21209031,21206332,20875091,20815382,20653589,20584027,20530805,20045384,19632671,19238200,19224546,19173597,19144550,18963030,18947761,18813873,18798627,18701925,18689548,18640931,18566984,18520680,18489160,18445598,18351694,18333613,18210019,17569403,17385849,17295779,16833741,16714129,16572194,16359978,16142842,15905890,15862240,15710580,15671438,15544735,15518358,15349899,15324765,14986336,14961045,14645754,14511591,14051827,13895282,12892232,12815257,12800116,12685186,12463861,12426868,11981889,10933057,10866634,10826886,10423358,10353859,10329235,10293294,9801103,9743183,9706882,9537599,9441876,9158682,9116006,9111625,8611125,7524639,7522148,4008619,3832526,3783062,3783061,2982741,2976940,2856500,2543327,2426199,2157479,2105054,1315167,30195625,25454304,23651750,21283739,21271845,38386713,38374255,37990447,37739311,37704750,37343553,37218128,36012358,36007540,35705560,35196489,35177690,34990589,34505572,34145292,33853348,33182643,33139798,32773036,32497071,32455661,32424346,31683990,31591221,31053729,30581147,30554962,30341039,29898327,29743178,29512652,27848971,27629970,27208311,27129231,27046124,26969721,26818732,26683934,26494233,26334888,25879842,25609138,25471051,25411371,24969772,24812553,24551982,24224794[uid]

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Novel homozygote variant in the HJV gene leading to juvenile hemochromatosis: a case report.

Ghanadi K, Mahmoudvand G, Karimi Rouzbahani A. Ghanadi K, et al. Gastroenterol Hepatol Bed Bench. 2023;16(4):441-444. doi: 10.22037/ghfbb.v16i4.2721. Gastroenterol Hepatol Bed Bench. 2023. PMID: 38313348 Free PMC article.

Juvenile Hemochromatosis in an Asymptomatic Patient-Importance of Early Diagnosis.

Nashed B, Fonseca C, Vander Pols W, Kumar S, Lyons H, Berman B, Guzzardo GM. Nashed B, et al. JPGN Rep. 2022 Jul 29;3(3):e228. doi: 10.1097/PG9.0000000000000228. eCollection 2022 Aug. JPGN Rep. 2022. PMID: 37168645 Free PMC article.

Juvenile Hemochromatosis With Non-transfused Hemolytic Anemia Caused by a De Novo PIEZO1 Gene Mutation.

Imashuku S, Suemori SI, Wakamatsu M, Okuno Y, Muramatsu H, Makino S, Miyoshi T, Chonabayashi K, Kanno H. Imashuku S, et al. J Pediatr Hematol Oncol. 2023 May 1;45(4):e510-e513. doi: 10.1097/MPH.0000000000002639. Epub 2023 Feb 21. J Pediatr Hematol Oncol. 2023. PMID: 36898020

Juvenile Hemochromatosis due to a Homozygous Variant in the HJV Gene.

Moreno-Risco MB, Méndez M, Moreno-Carralero MI, López-Moreno AM, Vagace-Valero JM, Morán-Jiménez MJ. Moreno-Risco MB, et al. Case Rep Pediatr. 2022 Apr 11;2022:7743748. doi: 10.1155/2022/7743748. eCollection 2022. Case Rep Pediatr. 2022. PMID: 35449524 Free PMC article.

Impact of HFE-2 and HAMP Gene Variations on Iron Overload in Pediatric Patients with Non-Transfusion Dependent Thalassemia: A Pilot Study.

Bharadwaj N, Peyam S, Bhatia P, Bhatia A, Das R, Singh M, Bansal D, Trehan A, Jain R. Bharadwaj N, et al. Indian J Hematol Blood Transfus. 2022 Jan;38(1):158-163. doi: 10.1007/s12288-021-01442-9. Epub 2021 May 7. Indian J Hematol Blood Transfus. 2022. PMID: 35125723 Free PMC article.

New Mutations in HFE2 and TFR2 Genes Causing Non HFE-Related Hereditary Hemochromatosis.

Hernández G, Ferrer-Cortès X, Venturi V, Musri M, Pilquil MF, Torres PMM, Rodríguez IH, Mínguez MÀR, Kelleher NJ, Pelucchi S, Piperno A, Alberca EP, Ricós GG, Giró EC, Pérez-Montero S, Tornador C, Villà-Freixa J, Sánchez M. Hernández G, et al. Genes (Basel). 2021 Dec 13;12(12):1980. doi: 10.3390/genes12121980. Genes (Basel). 2021. PMID: 34946929 Free PMC article.

Appropriate Clinical Genetic Testing of Hemochromatosis Type 2-4, Including Ferroportin Disease.

Kowdley DS, Kowdley KV. Kowdley DS, et al. Appl Clin Genet. 2021 Aug 12;14:353-361. doi: 10.2147/TACG.S269622. eCollection 2021. Appl Clin Genet. 2021. PMID: 34413666 Free PMC article. Review.

Performance of two prognostic scores that incorporate genetic information to predict long-term outcomes following resection of colorectal cancer liver metastases: An external validation of the MD Anderson and JHH-MSK scores.

Sasaki K, Gagnière J, Dupré A, Ardiles V, O'Connor JM, Wang J, Moro A, Morioka D, Buettner S, Gau L, Ribeiro M, Wagner D, Andreatos N, Løes IM, Fitschek F, Kaczirek K, Lønning PE, Kornprat P, Poultsides G, Kamphues C, Imai K, Baba H, Endo I, Kwon CHD, Aucejo FN, de Santibañes E, Kreis ME, Margonis GA. Sasaki K, et al. J Hepatobiliary Pancreat Sci. 2021 Jul;28(7):581-592. doi: 10.1002/jhbp.963. Epub 2021 Apr 24. J Hepatobiliary Pancreat Sci. 2021. PMID: 33797866

Juvenile Hemochromatosis: Rheumatic Manifestations of 2 Sisters Responding to Deferasirox Treatment. A Case Series and Literature Review.

Alqanatish J, Alsowailmi B, Alfarhan H, Alhamzah A, Alharbi T. Alqanatish J, et al. Open Access Rheumatol. 2021 Jan 15;13:15-21. doi: 10.2147/OARRR.S276112. eCollection 2021. Open Access Rheumatol. 2021. PMID: 33488128 Free PMC article.

Atypical juvenile hereditary hemochromatosis onset with positive pancreatic islet autoantibodies diabetes caused by novel mutations in HAMP and overall clinical management.

Wu HX, Liu JY, Yan DW, Li L, Zhuang XH, Li HY, Zhou ZG, Zhou HD. Wu HX, et al. Mol Genet Genomic Med. 2020 Dec;8(12):e1522. doi: 10.1002/mgg3.1522. Epub 2020 Oct 5. Mol Genet Genomic Med. 2020. PMID: 33016646 Free PMC article. Review.

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