BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

201 related articles for article (PubMed ID: 36187095)

  • 1. The diagnostic value of the olfactory evaluation for congenital hypogonadotropic hypogonadism.
    Yu B; Chen K; Mao J; Hou B; You H; Wang X; Nie M; Huang Q; Zhang R; Zhu Y; Sun B; Feng F; Zhou W; Wu X
    Front Endocrinol (Lausanne); 2022; 13():909623. PubMed ID: 36187095
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Olfactory function and olfactory bulbs in patients with Kallmann syndrome].
    Kokoreva KD; Chugunov IS; Vladimirova VP; Ivannikova TE; Bogdanov VP; Bezlepkina OB
    Probl Endokrinol (Mosk); 2023 May; 69(2):67-74. PubMed ID: 37448273
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Computed tomography of the anterior skull base in Kallmann syndrome reveals specific ethmoid bone abnormalities associated with olfactory bulb defects.
    Maione L; Benadjaoud S; Eloit C; Sinisi AA; Colao A; Chanson P; Ducreux D; Benoudiba F; Young J
    J Clin Endocrinol Metab; 2013 Mar; 98(3):E537-46. PubMed ID: 23348397
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Quantitative magnetic resonance imaging evaluation of the olfactory system in Kallmann syndrome: correlation with a clinical smell test.
    Koenigkam-Santos M; Santos AC; Versiani BR; Diniz PR; Junior JE; de Castro M
    Neuroendocrinology; 2011; 94(3):209-17. PubMed ID: 21606642
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An objective olfactory evaluation and its correlation with magnetic resonance imaging findings in Asian Indian patients with idiopathic hypogonadotropic hypogonadism.
    Jagtap VS; Sarathi V; Lila AR; Nair S; Bukan A; Sankhe SS; Shivane V; Bandgar T; Menon P; Shah NS
    Endocr Pract; 2013; 19(4):669-74. PubMed ID: 23512393
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Congenital hypogonadotropic hypogonadism and Kallmann syndrome in males].
    Ghervan C; Young J
    Presse Med; 2014 Feb; 43(2):152-61. PubMed ID: 24456696
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Correlation of Olfactory Phenotype by Indian Smell Identification Test and Quantitative MRI of Olfactory Apparatus in Idiopathic Hypogonadotropic Hypogonadism.
    Nehara HR; Sharma B; Kumar A; Saran S; Mangalhara NK; Mathur SK
    Indian J Endocrinol Metab; 2019; 23(3):367-372. PubMed ID: 31641641
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.
    Barraud S; Delemer B; Poirsier-Violle C; Bouligand J; Mérol JC; Grange F; Higel-Chaufour B; Decoudier B; Zalzali M; Dwyer AA; Acierno JS; Pitteloud N; Millar RP; Young J
    Neuroendocrinology; 2021; 111(1-2):99-114. PubMed ID: 32074614
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Olfactory dysfunction in children with Kallmann syndrome: relation of smell tests with brain magnetic resonance imaging.
    Anık A; Çatlı G; Abacı A; Güleryüz H; Güdücü Ç; Öniz A; Can Ş; Dündar B; Böber E
    Hormones (Athens); 2015; 14(2):293-9. PubMed ID: 25553765
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Reconsidering olfactory bulb magnetic resonance patterns in Kallmann syndrome.
    Hacquart T; Ltaief-Boudrigua A; Jeannerod C; Hannoun S; Raverot G; Pugeat M; Brac de la Perriere A; Lapras V; Nugues F; Dode C; Cotton F
    Ann Endocrinol (Paris); 2017 Oct; 78(5):455-461. PubMed ID: 28807454
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Reconsidering the olfactory and brain structures in Kallmann's syndrome: New findings in the analysis of volumetry.
    Bortolotto Felippe Trentin M; Borges Daniel K; Reis F; Adolfo Silva Junior N; Appenzeller S; Rittner L; Benetti Pinto C; Garmes HM
    Clin Endocrinol (Oxf); 2023 Apr; 98(4):554-558. PubMed ID: 36536529
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Whole Exome Sequencing Revealed a Novel Nonsense Variant in the GNRHR Gene Causing Normosmic Hypogonadotropic Hypogonadism in a Pakistani Family.
    Hussain HMJ; Murtaza G; Jiang X; Khan R; Khan M; Kakakhel MBS; Khan T; Wahab F; Zhang H; Zhang Y; Khan MB; Ahmed P; Ma H; Xu Z
    Horm Res Paediatr; 2019; 91(1):9-16. PubMed ID: 30947225
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Normal sense of smell in Kallmann syndrome. A case report].
    Wüstenberg EG; Fleischer A; Gerbert B; Abolmaali N; Hüttenbrink KB; Hummel T
    Laryngorhinootologie; 2001 Feb; 80(2):85-9. PubMed ID: 11253570
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Kallman syndrome versus idiopathic hypogonadotropic hypogonadism at MR imaging.
    Vogl TJ; Stemmler J; Heye B; Schopohl J; Danek A; Bergman C; Balzer JO; Felix R
    Radiology; 1994 Apr; 191(1):53-7. PubMed ID: 8134597
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sniffin' Sticks and olfactory system imaging in patients with Kallmann syndrome.
    Ottaviano G; Cantone E; D'Errico A; Salvalaggio A; Citton V; Scarpa B; Favaro A; Sinisi AA; Liuzzi R; Bonanni G; Di Salle F; Elefante A; Manara R; Staffieri A; Martini A; Brunetti A
    Int Forum Allergy Rhinol; 2015 Sep; 5(9):855-61. PubMed ID: 25951300
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Anatomic olfactory structural abnormalities in congenital smell loss: magnetic resonance imaging evaluation of olfactory bulb, groove, sulcal, and hippocampal morphology.
    Levy LM; Degnan AJ; Sethi I; Henkin RI
    J Comput Assist Tomogr; 2013; 37(5):650-7. PubMed ID: 24045236
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Biallelic PROKR2 variants and congenital hypogonadotropic hypogonadism: a case report and a literature review.
    Sugisawa C; Taniyama M; Sato T; Takahashi Y; Hasegawa T; Narumi S
    Endocr J; 2022 Jul; 69(7):831-838. PubMed ID: 35236788
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Expanding the genetic spectrum of ANOS1 mutations in patients with congenital hypogonadotropic hypogonadism.
    Gonçalves CI; Fonseca F; Borges T; Cunha F; Lemos MC
    Hum Reprod; 2017 Mar; 32(3):704-711. PubMed ID: 28122887
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism.
    Aoyama K; Mizuno H; Tanaka T; Togawa T; Negishi Y; Ohashi K; Hori I; Izawa M; Hamajima T; Saitoh S
    J Pediatr Endocrinol Metab; 2017 Oct; 30(10):1111-1118. PubMed ID: 28915117
    [TBL] [Abstract][Full Text] [Related]  

  • 20. X chromosome-linked Kallmann syndrome: clinical heterogeneity in three siblings carrying an intragenic deletion of the KAL-1 gene.
    Massin N; Pêcheux C; Eloit C; Bensimon JL; Galey J; Kuttenn F; Hardelin JP; Dodé C; Touraine P
    J Clin Endocrinol Metab; 2003 May; 88(5):2003-8. PubMed ID: 12727945
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.