PubMed for id: 384027

Year	Number of Results
1977	1
1990	1
1992	1
1993	2
1994	1
1996	1
1997	1
1998	2
1999	1
2000	5
2003	1
2005	1
2006	1
2007	2
2008	2
2009	4
2010	5
2011	7
2012	3
2013	5
2014	5
2015	2
2016	6
2017	6
2018	5
2019	6
2020	7
2021	3
2022	8
2023	6
2024	1

1

Overexpression of the orphan receptor Nur77 and its translocation induced by PCH4 may inhibit malignant glioma cell growth and induce cell apoptosis.

Chang LF, Lin PC, Ho LI, Liu PY, Wu WC, Chiang IP, Chang HW, Lin SZ, Harn YC, Harn HJ, Chiou TW. Chang LF, et al. J Surg Oncol. 2011 Apr;103(5):442-50. doi: 10.1002/jso.21809. Epub 2011 Jan 18. J Surg Oncol. 2011. PMID: 21246566

2

Severe, fetal-onset form of olivopontocerebellar hypoplasia in three sibs: PCH type 5?

Patel MS, Becker LE, Toi A, Armstrong DL, Chitayat D. Patel MS, et al. Am J Med Genet A. 2006 Mar 15;140(6):594-603. doi: 10.1002/ajmg.a.31095. Am J Med Genet A. 2006. PMID: 16470708

3

[Spinal muscular atrophy associated with olivopontocerebellar hypoplasia. A case report].

Serra-Ortega A, Torres A, Segreo M. Serra-Ortega A, et al. Rev Neurol. 2005 Jan 16-31;40(2):90-2. Rev Neurol. 2005. PMID: 15712162 Free article. Spanish.

4

Anterior horn cell disease and olivopontocerebellar hypoplasia.

Ryan MM, Cooke-Yarborough CM, Procopis PG, Ouvrier RA. Ryan MM, et al. Pediatr Neurol. 2000 Aug;23(2):180-4. doi: 10.1016/s0887-8994(00)00166-1. Pediatr Neurol. 2000. PMID: 11020648

5

Prenatal diagnosis of fatal infantile olivopontocerebellar hypoplasia syndrome.

Mitra AG, Salvino AR, Spence JE. Mitra AG, et al. Prenat Diagn. 1999 Apr;19(4):375-8. doi: 10.1002/(sici)1097-0223(199904)19:4<375::aid-pd528>3.0.co;2-j. Prenat Diagn. 1999. PMID: 10327146

6

Three siblings of fatal infantile encephalopathy with olivopontocerebellar hypoplasia and microcephaly.

Hashimoto K, Takeuchi Y, Kida Y, Hasegawa H, Kantake M, Sasaki A, Asanuma K, Isumi H, Takashima S. Hashimoto K, et al. Brain Dev. 1998 Apr;20(3):169-74. doi: 10.1016/s0387-7604(98)00014-x. Brain Dev. 1998. PMID: 9628193

7

Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly. Report of three siblings.

Albrecht S, Schneider MC, Belmont J, Armstrong DL. Albrecht S, et al. Acta Neuropathol. 1993;85(4):394-9. doi: 10.1007/BF00334450. Acta Neuropathol. 1993. PMID: 8480512

8

Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with cerebellar hypoplasia and disrupt Purkinje cell differentiation.

Coolen M, Altin N, Rajamani K, Pereira E, Siquier-Pernet K, Puig Lombardi E, Moreno N, Barcia G, Yvert M, Laquerrière A, Pouliet A, Nitschké P, Boddaert N, Rausell A, Razavi F, Afenjar A, Billette de Villemeur T, Al-Maawali A, Al-Thihli K, Baptista J, Beleza-Meireles A, Garel C, Legendre M, Gelot A, Burglen L, Moutton S, Cantagrel V. Coolen M, et al. Am J Hum Genet. 2022 May 5;109(5):909-927. doi: 10.1016/j.ajhg.2022.03.010. Epub 2022 Apr 6. Am J Hum Genet. 2022. PMID: 35390279 Free PMC article.

9

A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family.

Sepahvand A, Razmara E, Bitarafan F, Galehdari M, Tavasoli AR, Almadani N, Garshasbi M. Sepahvand A, et al. Mol Genet Genomic Med. 2020 Oct;8(10):e1413. doi: 10.1002/mgg3.1413. Epub 2020 Jul 22. Mol Genet Genomic Med. 2020. PMID: 32697043 Free PMC article.

10

Pontocerebellar hypoplasia type 2 and TSEN2: review of the literature and two novel mutations.

Bierhals T, Korenke GC, Uyanik G, Kutsche K. Bierhals T, et al. Eur J Med Genet. 2013 Jun;56(6):325-30. doi: 10.1016/j.ejmg.2013.03.009. Epub 2013 Apr 3. Eur J Med Genet. 2013. PMID: 23562994 Review.

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