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Ola Sandgren

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Chemicals & Drugs

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Sweden

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Physiology

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Vitreous Body

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TOP 3
Ainars Reinis; Irina Golovleva; Linda Köhn; Ola Sandgren
Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation.
Linda Köhn; Susanne Kohl; Sara J Bowne; Lori S Sullivan; Ulrich Kellner; Stephen P Daiger; Ola Sandgren; Irina Golovleva
PITPNM3 is an uncommon cause of cone and cone-rod dystrophies.
Irina Golovleva; Linda Köhn; Marie S I Burstedt; Stephen P Daiger; Ola Sandgren
Mutation spectra in autosomal dominant and recessive retinitis pigmentosa in northern Sweden.

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All Publications

2013: Ainars Reinis; Irina Golovleva; Linda Köhn; Ola Sandgren
Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation.
Acta ophthalmologica 2013;91(3):259-66.
2010: Linda Köhn; Susanne Kohl; Sara J Bowne; Lori S Sullivan; Ulrich Kellner; Stephen P Daiger; Ola Sandgren; Irina Golovleva
PITPNM3 is an uncommon cause of cone and cone-rod dystrophies.
Ophthalmic genetics 2010;31(3):139-40.
2010: Irina Golovleva; Linda Köhn; Marie S I Burstedt; Stephen P Daiger; Ola Sandgren
Mutation spectra in autosomal dominant and recessive retinitis pigmentosa in northern Sweden.
Advances in experimental medicine and biology 2010;664():255-62.
2008: Ola Sandgren; Daniel Kjellgren; Ole B Suhr
Ocular manifestations in liver transplant recipients with familial amyloid polyneuropathy.
Acta ophthalmologica 2008;86(5):520-4.
2008: Marie S I Burstedt; Ola Sandgren; Irina Golovleva; Lillemor Wachtmeister
Effects of prolonged dark adaptation in patients with retinitis pigmentosa of Bothnia type: an electrophysiological study.
Documenta ophthalmologica. Advances in ophthalmology 2008;116(3):193-205.
2008: Linda Köhn; Konstantin Kadzhaev; Marie S I Burstedt; Susann Haraldsson; Ola Sandgren; Irina Golovleva
Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families.
Advances in experimental medicine and biology 2008;613():229-34.
2007: Asa C Jonsson; Marie S I Burstedt; Irina Golovleva; Ola Sandgren
Tinted contact lenses in Bothnia dystrophy.
Acta ophthalmologica Scandinavica 2007;85(5):534-9.
2007: Linda Köhn; Konstantin Kadzhaev; Marie S I Burstedt; Susann Haraldsson; Bengt Hallberg; Ola Sandgren; Irina Golovleva
Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families.
European journal of human genetics : EJHG 2007;15(6):664-71.
2005: Gösta Holmgren; Urban Hellman; Hans-Eric Lundgren; Ola Sandgren; Ole B Suhr
Impact of homozygosity for an amyloidogenic transthyretin mutation on phenotype and long term outcome.
Journal of medical genetics 2005;42(12):953-6.
2005: Marie S I Burstedt; Eva Mönestam; Ola Sandgren
Associations between specific measures of vision and vision-related quality of life in patients with bothnia dystrophy, a defined type of retinitis pigmentosa.
Retina (Philadelphia, Pa.) 2005;25(3):317-23.
2003: Marie S I Burstedt; Ola Sandgren; Irina Golovleva; Lillemor Wachtmeister
Retinal function in Bothnia dystrophy. An electrophysiological study.
Vision research 2003;43(24):2559-71.
2003: Irina Golovleva; Sanjoy K Bhattacharya; Zhiping Wu; Natacha Shaw; Yanwu Yang; Khurshid Andrabi; Karen A West; Marie S I Burstedt; Kristina Forsman; Gösta Holmgren; Ola Sandgren; Noa Noy; Jun Qin; John W Crabb
Disease-causing mutations in the cellular retinaldehyde binding protein tighten and abolish ligand interactions.
The Journal of biological chemistry 2003;278(14):12397-402.
2002: Katsuki Haraoka; Yukio Ando; Eiko Ando; Ola Sandgren; Akira Hirata; Masaaki Nakamura; Hisayasu Terazaki; Takahiro Tajiri; Yutaka Tanoue; Xuguo Sun; Hiroaki Okabe; Hidenobu Tanihara
Amyloid deposition in ocular tissues of patients with familial amyloidotic polyneuropathy (FAP).
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2002;9(3):183-9.
2001: Marie S I Burstedt; Kristina Forsman-Semb; Irina Golovleva; T Janunger; Lillemor Wachtmeister; Ola Sandgren
Ocular phenotype of bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene.
Archives of ophthalmology 2001;119(2):260-7.
2000: Marijke Van Ghelue; H L Eriksen; Vesna Ponjavic; Toril Fagerheim; Sten Andréasson; Kristina Forsman-Semb; Ola Sandgren; Gösta Holmgren; Lisbeth Tranebjaerg
Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the family.
Ophthalmic genetics 2000;21(4):197-209.
2000: C Mambule; Yukio Ando; Intissar Anan; Gösta Holmgren; Ola Sandgren; T Stigbrandt; K Tashima; Ole B Suhr
Enhancement of AA-amyloid formation in mice by transthyretin amyloid fragments and polyethylene glycol.
Biochimica et biophysica acta 2000;1474(3):331-6.
1999: DG Stathakis; Nitin Udar; Ola Sandgren; sten andreasson; Peter J Bryant; K Small; Kristina Forsman-Semb
Genomic organization of human DLG4, the gene encoding postsynaptic density 95.
Journal of neurochemistry 1999;73(6):2250-65.
1999: Yukio Ando; Eiko Ando; Per-Ingvar Ohlsson; Anders Olofsson; Ola Sandgren; Ole B Suhr; Hisayasu Terazaki; Konen Obayashi; Erik Lundgren; Masayuki Ando; Akira Negi
Analysis of transthyretin amyloid fibrils from vitreous samples in familial amyloidotic polyneuropathy (Val30Met).
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 1999;6(2):119-23.
1999: Benjamin Bakall; Towa Marknell; Sofie Ingvast; M J Koisti; Ola Sandgren; W Li; A A Bergen; sten andreasson; Thomas Rosenberg; Konstantin Petrukhin; Claes Wadelius
The mutation spectrum of the bestrophin protein--functional implications.
Human genetics 1999;104(5):383-9.
1999: Marie S I Burstedt; Ola Sandgren; Gösta Holmgren; Kristina Forsman-Semb
Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26.
Investigative ophthalmology & visual science 1999;40(5):995-1000.
1998: Hideyo Inouye; F S Domingues; Ana M Damas; Maria João Saraiva; Erik Lundgren; Ola Sandgren; Daniel A Kirschner
Analysis of x-ray diffraction patterns from amyloid of biopsied vitreous humor and kidney of transthyretin (TTR) Met30 familial amyloidotic polyneuropathy (FAP) patients: axially arrayed TTR monomers constitute the protofilament.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 1998;5(3):163-74.
1998: Ulf Ekström; Sten Andréasson; Vesna Ponjavic; Magnus Abrahamson; Ola Sandgren; Peter Nilsson-Ehle; Berndt Ehinger
A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration.
Ophthalmic genetics 1998;19(3):149-56.
1998: Konstantin Petrukhin; M J Koisti; Benjamin Bakall; W Li; G Xie; Towa Marknell; Ola Sandgren; Kristina Forsman; G Holmgren; sten andreasson; M Vujic; A A Bergen; V McGarty-Dugan; David Figueroa; Christopher P Austin; Michael Metzker; CT Caskey; C Wadelius
Identification of the gene responsible for Best macular dystrophy.
Nature genetics 1998;19(3):241-7.
1998: Jens Johansson; Lars Forsgren; Ola Sandgren; Alexis Brice; Gösta Holmgren; M Holmberg
Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation.
Human molecular genetics 1998;7(2):171-6.
1997: C Graff; A Eriksson; Kristina Forsman; Ola Sandgren; Gösta Holmgren; Claes Wadelius
Refined genetic localization of the Best disease gene in 11q13 and physical mapping of linked markers on radiation hybrids.
Human genetics 1997;101(3):263-70.
1997: Herbert Sandstrom; Ake Wahlin; M Eriksson; Gösta Holmgren; L Lind; Ola Sandgren
Angioid streaks are part of a familial syndrome of dyserythropoietic anaemia (CDA III).
British journal of haematology 1997;98(4):845-9.
1997: G Goldsteins; Karin Andersson; Anders Olofsson; Ingrid Dacklin; A Edvinsson; Vladimir Baranov; Ola Sandgren; C Thylén; S Hammarstrom; Erik Lundgren
Characterization of two highly amyloidogenic mutants of transthyretin.
Biochemistry 1997;36(18):5346-52.
1996: L Forsgren; R Libelius; M Holmberg; Ulrika von Döbeln; R Wibom; J Heijbel; Ola Sandgren; Gösta Holmgren
Muscle morphology and mitochondrial investigations of a family with autosomal dominant cerebellar ataxia and retinal degeneration mapped to chromosome 3p12-p21.1.
Journal of the neurological sciences 1996;144(1-2):91-8.
1996: Yukio Ando; Per-Ingvar Ohlsson; Ole B Suhr; N Nyhlin; Takeshi Yamashita; Gösta Holmgren; A Danielsson; Ola Sandgren; Makoto Uchino; Masayuki Ando
A new simple and rapid screening method for variant transthyretin-related amyloidosis.
Biochemical and biophysical research communications 1996;228(2):480-3.
1995: J Balciuniene; K Johansson; Ola Sandgren; L Wachtmeister; Gösta Holmgren; Kristina Forsman
A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13.
Genomics 1995;30(2):281-6.
1995: Ola Sandgren
Ocular amyloidosis, with special reference to the hereditary forms with vitreous involvement.
Survey of ophthalmology 1995;40(3):173-96.
1995: M Holmberg; J Johansson; L Forsgren; J Heijbel; Ola Sandgren; Gösta Holmgren
Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1.
Human molecular genetics 1995;4(8):1441-5.
1994: C Graff; Kristina Forsman; C Larsson; S Nordström; L Lind; K Johansson; Ola Sandgren; J Weissenbach; Gösta Holmgren; Karl-Henrik Gustavson
Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci.
Genomics 1994;24(3):425-34.
1993: A Sousa; R Andersson; U Drugge; Gösta Holmgren; Ola Sandgren
Familial amyloidotic polyneuropathy in Sweden: geographical distribution, age of onset, and prevalence.
Human heredity 1993;43(5):288-94.
1993: U Drugge; R Andersson; F Chizari; M Danielsson; Gösta Holmgren; Ola Sandgren; A Sousa
Familial amyloidotic polyneuropathy in Sweden: a pedigree analysis.
Journal of medical genetics 1993;30(5):388-92.
1993: J A Hamilton; LK Steinrauf; Bradford C Braden; Juris J Liepnieks; Merrill D Benson; Gösta Holmgren; Ola Sandgren; L Steen
The x-ray crystal structure refinements of normal human transthyretin and the amyloidogenic Val-30-->Met variant to 1.7-A resolution.
The Journal of biological chemistry 1993;268(4):2416-24.
1993: C Thylén; J Wahlqvist; E Haettner; Ola Sandgren; G Holmgren; E Lundgren
Modifications of transthyretin in amyloid fibrils: analysis of amyloid from homozygous and heterozygous individuals with the Met30 mutation.
The EMBO journal 1993;12(2):743-8.
1992: J A Hamilton; LK Steinrauf; Juris J Liepnieks; Merrill D Benson; Gösta Holmgren; Ola Sandgren; L Steen
Alteration in molecular structure which results in disease: the Met-30 variant of human plasma transthyretin.
Biochimica et biophysica acta 1992;1139(1-2):9-16.
1992: Gösta Holmgren; S Bergström; U Drugge; E Lundgren; C Nording-Sikström; Ola Sandgren; L Steen
Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences.
Clinical genetics 1992;41(1):39-41.
1991: Ola Sandgren; U Drugge; Gösta Holmgren; A Sousa
Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study.
Clinical genetics 1991;40(6):452-60.
1990: Ola Sandgren; Gösta Holmgren; E Lundgren
Vitreous amyloidosis associated with homozygosity for the transthyretin methionine-30 gene.
Archives of ophthalmology 1990;108(11):1584-6.
1990: Ola Sandgren; P A Hofer
Conjunctival involvement in familial amyloidotic polyneuropathy.
Acta ophthalmologica 1990;68(3):292-6.
1988: Gösta Holmgren; U Drugge; E Lundgren; Ola Sandgren; L Steen
[Identification of genetic carriers in familial amyloidosis with polyneuropathy is possible with the DNA technic].
Läkartidningen 1988;85(44):3677-9.
1988: Gösta Holmgren; E Haettner; I Nordenson; Ola Sandgren; L Steen; E Lundgren
Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy.
Clinical genetics 1988;34(5):333-8.
1988: Ola Sandgren; Gösta Holmgren; E Lundgren; L Steen
Restriction fragment length polymorphism analysis of mutated transthyretin in vitreous amyloidosis.
Archives of ophthalmology 1988;106(6):790-2.
1988: Gösta Holmgren; E Holmberg; Anton Lindström; E Lindström; I Nordenson; Ola Sandgren; L Steen; B Svensson; E Lundgren; A von Gabain
Diagnosis of familial amyloidotic polyneuropathy in Sweden by RFLP analysis.
Clinical genetics 1988;33(3):176-80.
1983: Bert-Ove Olofsson; R Andersson; L Benson; S Blom; P A Hofer; Ola Sandgren; L Steen
[Familial amyloidosis with polyneuropathy in Sweden - a review].
Läkartidningen 1983;80(41):3785-7.