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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1957 1
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1964 6
1965 6
1966 9
1967 12
1968 9
1969 5
1970 19
1971 26
1972 45
1973 35
1974 34
1975 49
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1977 37
1978 40
1979 44
1980 46
1981 33
1982 50
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1984 32
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1986 35
1987 33
1988 24
1989 29
1990 36
1991 21
1992 30
1993 26
1994 22
1995 17
1996 27
1997 19
1998 18
1999 32
2000 35
2001 20
2002 22
2003 22
2004 23
2005 20
2006 16
2007 31
2008 15
2009 18
2010 22
2011 30
2012 33
2013 35
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2016 26
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2022 26
2023 24
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1,620 results

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Page 1
Chediak-Higashi syndrome.
Talbert ML, Malicdan MCV, Introne WJ. Talbert ML, et al. Curr Opin Hematol. 2023 Jul 1;30(4):144-151. doi: 10.1097/MOH.0000000000000766. Epub 2023 Apr 25. Curr Opin Hematol. 2023. PMID: 37254856 Free PMC article. Review.
PURPOSE OF REVIEW: Chediak-Higashi syndrome is a rare autosomal recessive disorder characterized by congenital immunodeficiency, bleeding diathesis, pyogenic infection, partial oculocutaneous albinism, and progressive neurodegeneration. ...This review serves …
PURPOSE OF REVIEW: Chediak-Higashi syndrome is a rare autosomal recessive disorder characterized by congenital immunode …
Chediak-Higashi syndrome.
Barak Y, Nir E. Barak Y, et al. Am J Pediatr Hematol Oncol. 1987 Spring;9(1):42-55. doi: 10.1097/00043426-198721000-00008. Am J Pediatr Hematol Oncol. 1987. PMID: 3296821 Review.
The use of cytochemical, electron microscopic, immunofluorescent, and tissue culture techniques has led to important advances in our understanding of the mechanisms underlying the pathogenesis of the Chediak-Higashi syndrome (CHS). This rare and fatal autosom …
The use of cytochemical, electron microscopic, immunofluorescent, and tissue culture techniques has led to important advances in our underst …
Chediak-Higashi syndrome.
Kaplan J, De Domenico I, Ward DM. Kaplan J, et al. Curr Opin Hematol. 2008 Jan;15(1):22-9. doi: 10.1097/MOH.0b013e3282f2bcce. Curr Opin Hematol. 2008. PMID: 18043242 Review.
PURPOSE OF REVIEW: Chediak-Higashi syndrome, a rare autosomal recessive disorder, was described over 50 years ago. ...This review will discuss the advances made in understanding the clinical aspects of the syndrome and the function of CHS1/LYST/Beige. …
PURPOSE OF REVIEW: Chediak-Higashi syndrome, a rare autosomal recessive disorder, was described over 50 years ago. ...T …
Chediak-Higashi Syndrome.
Mozafari R, Rajabnia M, Naleini SN. Mozafari R, et al. Arch Iran Med. 2019 Nov 1;22(11):673-674. Arch Iran Med. 2019. PMID: 31823635 No abstract available.
Chediak Higashi Syndrome with Hemophagocytic Lymphohistiocytosis.
Safavi M, Parvaneh N. Safavi M, et al. Fetal Pediatr Pathol. 2023 Apr;42(2):259-262. doi: 10.1080/15513815.2022.2077489. Epub 2022 May 24. Fetal Pediatr Pathol. 2023. PMID: 35608383
INTRODUCTION: Chediak-Higashi syndrome (CHS) is caused by dysfunction of lysosomal trafficking and presents with hypopigmentation, bleeding tendencies, neurological symptoms, and NK cell dysfunction. ...
INTRODUCTION: Chediak-Higashi syndrome (CHS) is caused by dysfunction of lysosomal trafficking and presents with hypopi …
Chediak Higashi syndrome with acute kidney injury: Questions.
Kalra S, Khera S, Sharma A, Daryani H, Singh V. Kalra S, et al. Pediatr Nephrol. 2022 Jun;37(6):1313-1315. doi: 10.1007/s00467-021-05404-1. Epub 2022 Jan 18. Pediatr Nephrol. 2022. PMID: 35041038 No abstract available.
Chediak-Higashi syndrome presenting as a hereditary spastic paraplegia.
Koh K, Tsuchiya M, Ishiura H, Shimazaki H, Nakamura T, Hara H, Suzuyama K, Takahashi M, Tsuji S, Takiyama Y; Japan Spastic Paraplegia Research Consortium. Koh K, et al. J Hum Genet. 2022 Feb;67(2):119-121. doi: 10.1038/s10038-021-00977-z. Epub 2021 Sep 6. J Hum Genet. 2022. PMID: 34483340
Hereditary spastic paraplegias (HSPs) comprise a group of neurodegenerative disorders characterized by weakness and leg spasticity. LYST is responsible for Chediak-Higashi syndrome (CHS), which exhibits partial oculocutaneous albinism, primary immunodeficienc …
Hereditary spastic paraplegias (HSPs) comprise a group of neurodegenerative disorders characterized by weakness and leg spasticity. LYST is …
Chediak Higashi syndrome with acute kidney injury: Answers.
Kalra S, Khera S, Sharma A, Daryani H, Singh V. Kalra S, et al. Pediatr Nephrol. 2022 Jun;37(6):1317-1318. doi: 10.1007/s00467-021-05414-z. Epub 2022 Jan 18. Pediatr Nephrol. 2022. PMID: 35041039 No abstract available.
Chediak-Higashi syndrome: Lessons from a single-centre case series.
Carneiro IM, Rodrigues A, Pinho L, de Jesus Nunes-Santos C, de Barros Dorna M, Moschione Castro APB, Pastorino AC. Carneiro IM, et al. Allergol Immunopathol (Madr). 2019 Nov-Dec;47(6):598-603. doi: 10.1016/j.aller.2019.04.010. Epub 2019 Aug 30. Allergol Immunopathol (Madr). 2019. PMID: 31477396
BACKGROUND: Chediak-Higashi syndrome (CHS) is a rare and potentially fatal autosomal recessive disease characterized by frequent bacterial infections, bleeding tendency, oculocutaneous albinism, photosensitivity and progressive neurologic dysfunction. ...
BACKGROUND: Chediak-Higashi syndrome (CHS) is a rare and potentially fatal autosomal recessive disease characterized by …
Oral manifestations of Chediak-Higashi syndrome: A systematic review.
de Arruda JAA, Sousa-Neto SS, Abreu LG, Schuch LF, Souza VG, Alves TVL, Martins-Andrade B, Shetty SS, Monteiro JLGC, Mendonça EF, Mesquita RA, Callou G. de Arruda JAA, et al. Dis Mon. 2023 Jan;69(1):101356. doi: 10.1016/j.disamonth.2022.101356. Epub 2022 Apr 10. Dis Mon. 2023. PMID: 35414415
Chediak-Higashi syndrome (CHS) is an autosomal recessive disorder characterized by leukocytes with giant secretory granules and a myriad of clinical features. However, it is unknown whether oral lesions are part of the syndrome or are refractory to sys …
Chediak-Higashi syndrome (CHS) is an autosomal recessive disorder characterized by leukocytes with giant secretory gran …
1,620 results