166 related articles for article (PubMed ID: 37155088)
1. A Review of Brain and Pituitary Gland MRI Findings in Patients with Ataxia and Hypogonadism.
Scaravilli A; Tranfa M; Pontillo G; Brais B; De Michele G; La Piana R; Saccà F; Santorelli FM; Synofzik M; Brunetti A; Cocozza S
Cerebellum; 2024 Apr; 23(2):757-774. PubMed ID: 37155088
[TBL] [Abstract][Full Text] [Related]
2. Conventional MRI findings in hereditary degenerative ataxias: a pictorial review.
Cocozza S; Pontillo G; De Michele G; Di Stasi M; Guerriero E; Perillo T; Pane C; De Rosa A; Ugga L; Brunetti A
Neuroradiology; 2021 Jul; 63(7):983-999. PubMed ID: 33733696
[TBL] [Abstract][Full Text] [Related]
3. [Cerebellar ataxia with hypogonadotropic hypogonadism and mental disturbance].
Johkura K; Yamaguchi S; Matsumoto M; Nagatomo H; Hasegawa O; Kuroiwa Y
No To Shinkei; 1994 May; 46(5):493-6. PubMed ID: 8060689
[TBL] [Abstract][Full Text] [Related]
4. [A woman with cerebellar ataxia and hypergonadotropic hypogonadism].
Wada S; Takaoka T; Kasama S; Kimura T; Kajiyama K; Takeda M; Yoshikawa H
Rinsho Shinkeigaku; 2010 Jan; 50(1):20-3. PubMed ID: 20120350
[TBL] [Abstract][Full Text] [Related]
5. Hypergonadotropic hypogonadism and hypersegmented neutrophils in a patient with ataxia-telangiectasia-like disorder: potential diagnostic clues?
Yoshida T; Awaya T; Shibata M; Kato T; Numabe H; Kobayashi J; Komatsu K; Heike T
Am J Med Genet A; 2014 Jul; 164A(7):1830-4. PubMed ID: 24733832
[TBL] [Abstract][Full Text] [Related]
6. Multiple pituitary hormone deficiencies in a patient with spinocerebellar ataxia: magnetic resonance imaging and hormonal studies.
Bhatia E; Shukla R; Gupta RK; Misra UK
J Endocrinol Invest; 1993 Sep; 16(8):639-42. PubMed ID: 8258653
[TBL] [Abstract][Full Text] [Related]
7. Different Cerebellar Ataxia Phenotypes Associated with Mutations of the PNPLA6 Gene in Brazilian Patients with Recessive Ataxias.
Teive HAG; Camargo CHF; Sato MT; Shiokawa N; Boguszewski CL; Raskin S; Buck C; Seminara SB; Munhoz RP
Cerebellum; 2018 Jun; 17(3):380-385. PubMed ID: 29248984
[TBL] [Abstract][Full Text] [Related]
8. STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations.
Hayer SN; Deconinck T; Bender B; Smets K; Züchner S; Reich S; Schöls L; Schüle R; De Jonghe P; Baets J; Synofzik M
Orphanet J Rare Dis; 2017 Feb; 12(1):31. PubMed ID: 28193273
[TBL] [Abstract][Full Text] [Related]
9. Hypomyelination, hypogonadotropic hypogonadism, hypodontia - First Polish patient.
Bekiesinska-Figatowska M; Mierzewska H; Kuczynska-Zardzewialy A; Szczepanik E; Obersztyn E
Brain Dev; 2010 Aug; 32(7):574-8. PubMed ID: 19700253
[TBL] [Abstract][Full Text] [Related]
10. Spinocerebellar ataxia and hypergonadotropic hypogonadism associated with familial sensorineural hearing loss.
Georgopoulos NA; Papapetropoulos S; Chroni E; Papadeas ES; Dimopoulos PA; Kyriazopoulout V; Davis MB; Eunson L; Kourounis G; Tzingounist VA
Gynecol Endocrinol; 2004 Aug; 19(2):105-10. PubMed ID: 15624272
[TBL] [Abstract][Full Text] [Related]
11. Hypergonadotropic hypogonadism in spinocerebellar ataxia type 2: a case report.
Kwon DY; Park MH
J Sex Med; 2009 Jun; 6(6):1779-1782. PubMed ID: 19473475
[TBL] [Abstract][Full Text] [Related]
12. SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: a large multi-centre study.
Synofzik M; Smets K; Mallaret M; Di Bella D; Gallenmüller C; Baets J; Schulze M; Magri S; Sarto E; Mustafa M; Deconinck T; Haack T; Züchner S; Gonzalez M; Timmann D; Stendel C; Klopstock T; Durr A; Tranchant C; Sturm M; Hamza W; Nanetti L; Mariotti C; Koenig M; Schöls L; Schüle R; de Jonghe P; Anheim M; Taroni F; Bauer P
Brain; 2016 May; 139(Pt 5):1378-93. PubMed ID: 27086870
[TBL] [Abstract][Full Text] [Related]
13. PITUITARY IMAGING BY MRI AND ITS CORRELATION WITH BIOCHEMICAL PARAMETERS IN THE EVALUATION OF MEN WITH HYPOGONADOTROPIC HYPOGONADISM.
Das G; Surya A; Okosieme O; Vali A; Tennant BP; Geen J; Abusahmin H
Endocr Pract; 2019 Sep; 25(9):926-934. PubMed ID: 31170366
[No Abstract] [Full Text] [Related]
14. New variant of familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafness.
Amor DJ; Delatycki MB; Gardner RJ; Storey E
Am J Med Genet; 2001 Feb; 99(1):29-33. PubMed ID: 11170090
[TBL] [Abstract][Full Text] [Related]
15. [Significance of neuroimaging in the diagnosis of Boucher-Neuhauser syndrome].
Santos AV; Saraiva PF; Breia PN
Acta Med Port; 2003; 16(3):193-5. PubMed ID: 12868401
[TBL] [Abstract][Full Text] [Related]
16. Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan.
Chiu HH; Hsaio CT; Tsai YS; Liao YC; Lee YC; Soong BW
Cerebellum; 2020 Aug; 19(4):544-549. PubMed ID: 32367277
[TBL] [Abstract][Full Text] [Related]
17. Co-occurrence of mutations in KIF7 and KIAA0556 in Joubert syndrome with ocular coloboma, pituitary malformation and growth hormone deficiency: a case report and literature review.
Niceta M; Dentici ML; Ciolfi A; Marini R; Barresi S; Lepri FR; Novelli A; Bertini E; Cappa M; Digilio MC; Dallapiccola B; Tartaglia M
BMC Pediatr; 2020 Mar; 20(1):120. PubMed ID: 32164589
[TBL] [Abstract][Full Text] [Related]
18. Ataxia and Hypogonadism: a Review of the Associated Genes and Syndromes.
De Michele G; Maione L; Cocozza S; Tranfa M; Pane C; Galatolo D; De Rosa A; De Michele G; Saccà F; Filla A
Cerebellum; 2024 Apr; 23(2):688-701. PubMed ID: 36997834
[TBL] [Abstract][Full Text] [Related]
19. Neuroimaging in cerebellar ataxia in childhood: A review.
Serrallach BL; Orman G; Boltshauser E; Hackenberg A; Desai NK; Kralik SF; Huisman TAGM
J Neuroimaging; 2022 Sep; 32(5):825-851. PubMed ID: 35749078
[TBL] [Abstract][Full Text] [Related]
20. FAMILIAL CEREBELLAR ATAXIA AND HYPOGONADISM.
MATTHEWS WB; RUNDLE AT
Brain; 1964 Sep; 87():463-8. PubMed ID: 14215172
[No Abstract] [Full Text] [Related]
[Next] [New Search]
