BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 35668006)

  • 1. 46 XY disorder of sex development (DSD) due to 5 alpha (SRD5A2) deficiency - Experience from a multidisciplinary Pediatric Gender Clinic.
    Bose S; Das K; George B; Raman V; Shubha AM; Mahadevappa K; Kumar P; Bantwal G; Ayyar V; Deb M
    J Pediatr Urol; 2022 Aug; 18(4):492.e1-492.e8. PubMed ID: 35668006
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency.
    Sasaki G; Ishii T; Hori N; Amano N; Homma K; Sato S; Hasegawa T
    Endocr J; 2019 Sep; 66(9):837-842. PubMed ID: 31178538
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in
    Akcan N; Uyguner O; Baş F; Altunoğlu U; Toksoy G; Karaman B; Avcı Ş; Yavaş Abalı Z; Poyrazoğlu Ş; Aghayev A; Karaman V; Bundak R; Başaran S; Darendeliler F
    J Clin Res Pediatr Endocrinol; 2022 Jun; 14(2):153-171. PubMed ID: 35135181
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Unexpected ethical dilemmas in sex assignment in 46,XY DSD due to 5-alpha reductase type 2 deficiency.
    Byers HM; Mohnach LH; Fechner PY; Chen M; Thomas IH; Ramsdell LA; Shnorhavorian M; McCauley EA; Amies Oelschlager AE; Park JM; Sandberg DE; Adam MP; Keegan CE
    Am J Med Genet C Semin Med Genet; 2017 Jun; 175(2):260-267. PubMed ID: 28544750
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene.
    Deeb A; Al Suwaidi H; Ibukunoluwa F; Attia S
    J Clin Res Pediatr Endocrinol; 2016 Jun; 8(2):236-40. PubMed ID: 27086719
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recognition of 5α-reductase-2 deficiency in an adult female 46XY DSD clinic.
    Berra M; Williams EL; Muroni B; Creighton SM; Honour JW; Rumsby G; Conway GS
    Eur J Endocrinol; 2011 Jun; 164(6):1019-25. PubMed ID: 21402750
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Etiological diagnosis of undervirilized male/XY disorder of sex development.
    Atta I; Ibrahim M; Parkash A; Lone SW; Khan YN; Raza J
    J Coll Physicians Surg Pak; 2014 Oct; 24(10):714-8. PubMed ID: 25327912
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Correlation of androgen receptor and SRD5A2 gene mutations with pediatric hypospadias in 46, XY DSD children.
    Fu XH; Zhang WQ; Qu XS
    Genet Mol Res; 2016 Mar; 15(1):15018232. PubMed ID: 27051040
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotype, genotype and gender identity in a large cohort of patients from India with 5α-reductase 2 deficiency.
    Shabir I; Khurana ML; Joseph AA; Eunice M; Mehta M; Ammini AC
    Andrology; 2015 Nov; 3(6):1132-9. PubMed ID: 26453174
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Molecular Basis of 5α-Reductase Type 2 Deficiency.
    Batista RL; Mendonca BB
    Sex Dev; 2022; 16(2-3):171-183. PubMed ID: 35793650
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Preliminary report: Surgical outcomes following genitoplasty in children with moderate to severe genital atypia.
    Bernabé KJ; Nokoff NJ; Galan D; Felsen D; Aston CE; Austin P; Baskin L; Chan YM; Cheng EY; Diamond DA; Ellens R; Fried A; Greenfield S; Kolon T; Kropp B; Lakshmanan Y; Meyer S; Meyer T; Delozier AM; Mullins LL; Palmer B; Paradis A; Reddy P; Reyes KJS; Schulte M; Swartz JM; Yerkes E; Wolfe-Christensen C; Wisniewski AB; Poppas DP
    J Pediatr Urol; 2018 Apr; 14(2):157.e1-157.e8. PubMed ID: 29398588
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ambiguous external genitalia due to defect of 5-α-reductase in seven Iraqi patients: prevalence of a novel mutation.
    Di Marco C; Bulotta AL; Varetti C; Dosa L; Michelucci A; Baldinotti F; Meucci D; Castagnini C; Lo Rizzo C; Di Maggio G; Simi P; Mari F; Bertelloni S; Renieri A; Messina M
    Gene; 2013 Sep; 526(2):490-3. PubMed ID: 23664981
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 5α-Reductase-2 deficiency: is gender assignment recommended in infancy? Two case-reports and review of the literature.
    Cocchetti C; Ristori J; Mazzoli F; Prunas A; Bertelloni S; Magini A; Vignozzi L; Maggi M; Fisher AD
    J Endocrinol Invest; 2020 Aug; 43(8):1131-1136. PubMed ID: 32036582
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 46,XY disorder of sex development (DSD) due to 17β-hydroxysteroid dehydrogenase type 3 deficiency.
    Mendonca BB; Gomes NL; Costa EM; Inacio M; Martin RM; Nishi MY; Carvalho FM; Tibor FD; Domenice S
    J Steroid Biochem Mol Biol; 2017 Jan; 165(Pt A):79-85. PubMed ID: 27163392
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Analysis of clinical phenotype and genotype of Chinese children with disorders of sex development].
    Lin H; Yang H; Fu JF; Yuan K; Huang W; Wu GP; Dong GJ; Tian DH; Wu DX; Tang DW; Wu LY; Sun YL; Pi LJ; Liu LP; Shi W; Gu LG; Huang ZH; Wang LQ; Chen HY; Li Y; Yu HY; Wei XR; Cheng XO; Shan Y; Liu X; Xu S; Liu XP; Luo YF; Xiao Y; Yang GM; Li M; Feng XQ; Ma DX; Pan JY; Tang RM; Chen R; Maimaiti DY; Liu XH; Cui Z; Su ZQ; Dong L; Zou YL; Liu J; Wu KX; Li Y; Li Y
    Zhonghua Er Ke Za Zhi; 2022 May; 60(5):435-441. PubMed ID: 35488637
    [No Abstract]   [Full Text] [Related]  

  • 16. [Preliminary investigation of gender assignment in 46,XY disorders of sex development with severe male undermasculinisation].
    Wu DH; Tian HJ; Yuan JN; Dong GP; Wu DW; Yang RW; Sun LY; Tang DX; Fu JF
    Zhonghua Er Ke Za Zhi; 2019 Oct; 57(10):786-791. PubMed ID: 31594066
    [No Abstract]   [Full Text] [Related]  

  • 17. Outcome of feminizing genital reconstruction in female sex assigned disorder of sex development in a low-income country.
    Ekenze SO; Chikani UN; Ezomike UO; Okafor DC
    J Pediatr Urol; 2019 May; 15(3):244-250. PubMed ID: 30926253
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New insights into 5α-reductase type 2 deficiency based on a multi-centre study: regional distribution and genotype-phenotype profiling of
    Gui B; Song Y; Su Z; Luo FH; Chen L; Wang X; Chen R; Yang Y; Wang J; Zhao X; Fan L; Liu X; Wang Y; Chen S; Gong C
    J Med Genet; 2019 Oct; 56(10):685-692. PubMed ID: 31186340
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutational analysis of compound heterozygous mutation p.Q6X/p.H232R in SRD5A2 causing 46,XY disorder of sex development.
    Li L; Zhang J; Li Q; Qiao L; Li P; Cui Y; Li S; Hao S; Wu T; Liu L; Yin J; Hu P; Dou X; Li S; Yang H
    Ital J Pediatr; 2022 Mar; 48(1):47. PubMed ID: 35331321
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Gender selection and postoperative follow-up analysis in 85 children with 46, XY disorders of sex development].
    Zhao M; Gong CX; Liang AM; Song YN; Liu Y; Wang JL; Ma Y; Ji WJ
    Zhonghua Er Ke Za Zhi; 2019 Jun; 57(6):434-439. PubMed ID: 31216800
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.