PubMed for id: 414129

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38284966,38267311,38091642,38016422,37865978,37315767,34237302,29532034,11152145,6890944,1456296,38680020,38679724,38679587,38679482,38678611,38678424,38678345,38678059,38676203,38675991,38675958,38675896,38675887,38675854,38675833,38674931,38674857,38674452,38674450,38674447,38674442,38674434,38674428,38674426,38674423,38674408,38674397,38674395,38674382,38674380,38674375,38674371,38674365,38674361,38674358,38674071,38674044,38674009,38673966,38673878,38673876,38672523,38672521,38672488,38672484,38672463,38672461,38672417,38672413,38671566,38671472,38671463,38671013,38670961,38670948,38670716,38670586,38669634,38669389,38669367,38668754,38668051,38668037,38666607,38666359,38664779,38664733,38664418,38664339,38662754,38662716,38662679,38661383,38660906,38659011,38658823,38658687,38658636,38656651,38655849,38655812,38655690,38655493,38654924,38654395,38654356,38654225,38654044,38653846,38653789,38653565,38652475,38652464,38650129,38649998,38649973,38649918,38649898,38645867,38644962,38644511,38644284,38644281,38643142,38642933,38642164,38642155,38641933,38641668,38640601,38639795,38639155,38638480,38637876,38637854,38637827,38637559,38635656,38634215,38633760,38633264,38633254,38633156,38632656,38632591,38632524,38632312,38631766,38630025,38629201,38628584,38627861,38627844,38627815,38627775,38627644,38627621,38627095,38627049,38625590,38625436,38623803,38623684,38623671,38622573,38622524,38622191,38622020,38621915,38621910,38621141,38619739,38617829,38617006,38616927,38616716,38616334,38614778,38614530,38613865,38613342,38613207,38612920,38612901,38612818,38612725,38612696,38612648,38612593,38612588,38612584,38612397,38610028,38609428,38609424,38608089,38607975,38607917,38607030,38607023,38607006,38606789,38606298,38605367,38605286,38605121,38604792,38604438,38603765,38603608,38602868,38602501,38602320,38601163,38600521,38600369,38598338,38598070,38598037,38598033,38597819,38597818,38597420,38596219,38595329,38594752,38594640,38594301,38594285,38591901,38591341,38591167,38590524,38590440,38589954,38589930,38589916,38589367,38589357,38589248,38588001,38587549,38587439,38586596,38586466,38586452,38584647,38584335,38584252,38584145,38581124,38580983,38580957,38580818,38579585,38579030,38578558,38578475,38578387,38578368,38578360,38578354,38578040,38577561,38575892,38575661,38575601,38575573,38574833,38574109,38573021,38572648,38572647,38572513,38572476,38571958,38570875,38570774,38570685,38570547,38570366,38569152,38569035,38568967,38568932,38568911,38568465,38567606,38567309,38566992,38566246,38566229,38566089,38565881,38565666,38565591,38565516,38565515,38565511,38565508,38565507,38565504,38564005,38563968,38563820,38563227,38562051,38562046,38561841,38561822,38561801,38561798,38561362,38561223,38560567,38558817,38558807,38558366,38557908,38557815,38557496,38557491,38556574,38556426,38556338,38556105,38555111,38555108,38554778,38554725,38553670,38553547,38553515,38553482,38553020,38552554,38552526,38552306,38552051,38552044,38551961,38551774,38551368,38550599,38550580,38548767,38548397,38548140,38547923,38547882,38547698,38547584,38547545,38547254,38547067,38547036,38546894,38546523,38546522,38546521,38546517,38546326,38546151,38546112,38544690,38544685,38543847,38543837,38543730,38543708,38542876,38542788,38542485,38542455,38542395,38542251,38542233,38542208,38542179,38542139,38542117,38542065,38541145,38540420,38540415,38540405,38540404,38540390,38540380,38540362,38540347,38540345,38540337,38540325,38539202,38539137,38539105,38538865,38538656,38538601,38538464,38537948,38537844,38537595,38537477,38537427,38536913,38536871,38536820,38536816,38536538,38536229,38534090,38533865,38532508,38532502,38532461,38531653,38530241,38530023,38529536,38529280,38529201,38528672,38528561,38528503,38528022,38527837,38527506,38527110,38526859,38526300,38526134,38525876,38524638,38524137,38523374,38522809,38522492,38522248,38521994,38521969,38521774,38521175,38520679,38520674,38520595,38520572,38520250,38519883,38519231,38519141,38518732,38518681,38518657,38518020,38517847,38517703,38517430,38517012,38516893,38516887,38516780,38516774,38516755,38515377,38515362,38515174,38515087,38514794,38514641,38514609,38514586,38514260,38514237,38512862,38512854,38512150,38511647,38511495,38511490,38511267,38510960,38510702,38510257,38509724,38509569,38509545,38509077,38508850,38508444,38508309,38507982,38507953,38507676,38507484,38506520,38506331,38506312,38506236,38506013,38505750,38504977,38504418,38504345,38504328,38503894,38503663,38503516[uid]

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Results by year

Year	Number of Results
1982	1
1992	1
2001	1
2018	1
2021	1
2023	7
2024	489

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The American Association for Thoracic Surgery (AATS) 2023 Expert Consensus Document: Recommendation for the care of children with trisomy 13 or trisomy 18 and a congenital heart defect.

St Louis JD, Bhat A, Carey JC, Lin AE, Mann PC, Smith LM, Wilfond BS, Kosiv KA, Sorabella RA, Alsoufi B. St Louis JD, et al. J Thorac Cardiovasc Surg. 2024 May;167(5):1519-1532. doi: 10.1016/j.jtcvs.2023.11.054. Epub 2024 Jan 27. J Thorac Cardiovasc Surg. 2024. PMID: 38284966

[Suspicion of constitutional abnormality at diagnosis of childhood leukemia: Update of the leukemia committee of the French Society of Childhood Cancers].

Strullu M, Cousin E, de Montgolfier S, Fenwarth L, Gachard N, Arnoux I, Duployez N, Girard S, Guilmatre A, Lafage M, Loosveld M, Petit A, Perrin L, Vial Y, Saultier P. Strullu M, et al. Bull Cancer. 2024 Mar;111(3):291-309. doi: 10.1016/j.bulcan.2023.11.011. Epub 2024 Jan 23. Bull Cancer. 2024. PMID: 38267311 French.

Cytogenetics in the management of myelodysplastic neoplasms (myelodysplastic syndromes, MDS): Guidelines from the groupe francophone de cytogénétique hématologique (GFCH).

Auger N, Douet-Guilbert N, Quessada J, Theisen O, Lafage-Pochitaloff M, Troadec MB. Auger N, et al. Curr Res Transl Med. 2023 Oct-Dec;71(4):103409. doi: 10.1016/j.retram.2023.103409. Epub 2023 Sep 17. Curr Res Transl Med. 2023. PMID: 38091642

Cytogenetics in the management of bone marrow failure syndromes: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH).

Cuccuini W, Collonge-Rame MA, Auger N, Douet-Guilbert N, Coster L, Lafage-Pochitaloff M. Cuccuini W, et al. Curr Res Transl Med. 2023 Oct-Dec;71(4):103423. doi: 10.1016/j.retram.2023.103423. Epub 2023 Oct 18. Curr Res Transl Med. 2023. PMID: 38016422

Cytogenetics in the management of hematologic neoplasms with germline predisposition: guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH).

Gachard N, Lafage-Pochitaloff M, Quessada J, Auger N, Collonge-Rame MA. Gachard N, et al. Curr Res Transl Med. 2023 Oct-Dec;71(4):103416. doi: 10.1016/j.retram.2023.103416. Epub 2023 Oct 21. Curr Res Transl Med. 2023. PMID: 37865978 Review.

Use of multi-gene panels in patients at high risk of hereditary digestive cancer: position statement of AEG, SEOM, AEGH and IMPaCT-GENÓMICA consortium.

Carballal S, Balaguer F, Bujanda L, Capellá G, González Santiago S, Jover R, Moreira L, Pineda M, Ruiz-Ponte C, Sánchez Heras AB, Serrano Blanch R, Soto JL, Vidal Tocino R, Cubiella J; en representación de AEG; SEOM; AEGH y consorcio IMPaCT-Genómica. Carballal S, et al. Gastroenterol Hepatol. 2024 Mar;47(3):293-318. doi: 10.1016/j.gastrohep.2023.06.004. Epub 2023 Jun 13. Gastroenterol Hepatol. 2024. PMID: 37315767 English, Spanish.

Recombinant SARS-CoV-2 envelope protein traffics to the trans-Golgi network following amphipol-mediated delivery into human cells.

Hutchison JM, Capone R, Luu DD, Shah KH, Hadziselimovic A, Van Horn WD, Sanders CR. Hutchison JM, et al. J Biol Chem. 2021 Aug;297(2):100940. doi: 10.1016/j.jbc.2021.100940. Epub 2021 Jul 5. J Biol Chem. 2021. PMID: 34237302 Free PMC article.

Mechanisms of KCNQ1 channel dysfunction in long QT syndrome involving voltage sensor domain mutations.

Huang H, Kuenze G, Smith JA, Taylor KC, Duran AM, Hadziselimovic A, Meiler J, Vanoye CG, George AL Jr, Sanders CR. Huang H, et al. Sci Adv. 2018 Mar 7;4(3):eaar2631. doi: 10.1126/sciadv.aar2631. eCollection 2018 Mar. Sci Adv. 2018. PMID: 29532034 Free PMC article.

A novel syndrome involving primary skeletal growth and retardation in siblings.

Hadziselimovic F, Fliegel CH, Miny P. Hadziselimovic F, et al. Clin Dysmorphol. 2001 Jan;10(1):33-6. doi: 10.1097/00019605-200101000-00007. Clin Dysmorphol. 2001. PMID: 11152145

A variant of the fra(X) syndrome.

Bühler EM, Hadziselimovic F, Pira U. Bühler EM, et al. Hum Genet. 1982;61(3):273-5. doi: 10.1007/BF00296460. Hum Genet. 1982. PMID: 6890944

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