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1Academic Journal
المؤلفون: Yamada K, Andrews C, Chan WM, McKeown CA, de Berardinis T, Loewenstein A, Lazar M, O'Keefe M, Letson R, London A, Ruttum M, Matsumoto N, Saito N, Morris L, Del Monte M, Johnson RH, Uyama E, Houtman WA, de Vries B, Carlow TJ, Hart BL, Krawiecki N, Shoffner J, Vogel MC, Katowitz J, Goldstein SM, Levin AV, Sener EC, Ozturk BT, Akarsu AN, Brodsky MC, Hanisch F, Cruse RP, Zubcov AA, Robb RM, Roggenkäemper P, Gottlob I, Kowal L, Battu R, Traboulsi EI, Franceschini P, Newlin A, Demer JL, Engle E.C., MAGLI, Adriano
المساهمون: Yamada, K, Andrews, C, Chan, Wm, Mckeown, Ca, Magli, Adriano, de Berardinis, T, Loewenstein, A, Lazar, M, O'Keefe, M, Letson, R, London, A, Ruttum, M, Matsumoto, N, Saito, N, Morris, L, Del Monte, M, Johnson, Rh, Uyama, E, Houtman, Wa, de Vries, B, Carlow, Tj, Hart, Bl, Krawiecki, N, Shoffner, J, Vogel, Mc, Katowitz, J, Goldstein, Sm, Levin, Av, Sener, Ec, Ozturk, Bt, Akarsu, An, Brodsky, Mc, Hanisch, F, Cruse, Rp, Zubcov, Aa, Robb, Rm, Roggenkäemper, P, Gottlob, I, Kowal, L, Battu, R, Traboulsi, Ei, Franceschini, P, Newlin, A, Demer, Jl, Engle, E. C.
Relation: firstpage:318; lastpage:321; journal:NATURE GENETICS; http://hdl.handle.net/11386/3305281
الاتاحة: http://hdl.handle.net/11386/3305281
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2Academic Journal
المؤلفون: Yamada, K, Andrews, C, Chan, WM, McKeown, CA, Magli, A, de Berardinis T, Loewenstein, A, Lazar, M, O'Keefe, M, Letson, R, London, A, Ruttum, M, Matsumoto, N, Saito, N, Morris, L, Del Monte M, Johnson, RH, Uyama, E, Houtman, WA, de Vries B, Carlow, TJ, Hart, BL, Krawiecki, N, Shoffner, J, Vogel, MC, Katowitz, J, Goldstein, SM, Levin, AV, Sener, EC, Ozturk, BT, Akarsu, AN, Brodsky, MC, Hanisch, F, Cruse, RP, Zubcov, AA, Robb, RM, Roggenkäemper, P, Gottlob, I, Kowal, L, Battu, R, Traboulsi, EI, Franceschini, P, Newlin, A, Demer, JL, Engle, EC
المصدر: PubMed ; http://www.ncbi.nlm.nih.gov/pubmed/
مصطلحات موضوعية: Amino Acid Sequence, Child, Female, Fibrosis, Genetic Linkage, Genetic Variation, Heterozygote, Humans, Kinesin, Male, Molecular Sequence Data, Mutation, Nerve Tissue Proteins, Oculomotor Muscles, Ophthalmoplegia, Pedigree, Phenotype, Sequence Homology, Amino Acid
وصف الملف: metadata
Relation: NAT GENET, 2003, 35 (4), pp. 318-321; http://hdl.handle.net/2381/17285; ng1261
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3Academic Journal
المؤلفون: SMITH, VC, POKORNY, J, DELLEMAN, JW, COZIJNSEN, M, Houtman, WA, WENT, LN
المصدر: SMITH , VC , POKORNY , J , DELLEMAN , JW , COZIJNSEN , M , Houtman , WA & WENT , LN 1983 , ' X-linked incomplete achromatopsia with more than one class of functional cones ' , Investigative ophthalmology & visual science , vol. 24 , no. 4 , pp. 451-457 .
وصف الملف: application/pdf
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4Academic Journal
المؤلفون: Oostra, RJ, Tijmes, NT, Cobben, JM, Bolhuis, PA, vanNesselrooij, BPM, Houtman, WA, deKokNazaruk, MM, BleekerWagemakers, EM
المصدر: Oostra , RJ , Tijmes , NT , Cobben , JM , Bolhuis , PA , vanNesselrooij , BPM , Houtman , WA , deKokNazaruk , MM & BleekerWagemakers , EM 1997 , ' On the many faces of Leber hereditary optic neuropathy ' , Clinical Genetics , vol. 51 , no. 6 , pp. 388-393 . ; ISSN:0009-9163
مصطلحات موضوعية: diagnostic criteria, genetic counselling, Leber hereditary optic neuropathy, mitochondrial DNA mutations, MITOCHONDRIAL-DNA MUTATION, GENOTYPE, PEDIGREES, FAMILY
الاتاحة: http://hdl.handle.net/11370/24f0d69e-7444-49fb-9818-dda996b43498
https://research.rug.nl/en/publications/on-the-many-faces-of-leber-hereditary-optic-neuropathy(24f0d69e-7444-49fb-9818-dda996b43498).html -
5Academic Journal
المؤلفون: Landesz, M, Worst, JGF, van Rij, G., Houtman, WA
المصدر: Landesz , M , Worst , JGF , van Rij , G & Houtman , WA 1997 , ' Opaque iris claw lens in a phakic eye to correct acquired diplopia ' , Journal of cataract and refractive surgery , vol. 23 , no. 1 , pp. 137-138 . https://doi.org/10.1016/S0886-3350(97)80166-6 ; ISSN:0886-3350
الاتاحة: http://hdl.handle.net/11370/ee83f28d-7408-4dd9-97b3-05bf455ed849
https://research.rug.nl/en/publications/opaque-iris-claw-lens-in-a-phakic-eye-to-correct-acquired-diplopia(ee83f28d-7408-4dd9-97b3-05bf455ed849).html
https://doi.org/10.1016/S0886-3350(97)80166-6 -
6Academic Journal
المؤلفون: Hordijk, R, VandeLogt, F, Houtman, WA, VanEssen, AJ
المصدر: Hordijk , R , VandeLogt , F , Houtman , WA & VanEssen , AJ 1996 , ' Chorioretinal dysplasia-microcephaly-mental retardation syndrome : Another family with autosomal dominant inheritance ' , Genetic counseling , vol. 7 , no. 2 , pp. 113-122 .
مصطلحات موضوعية: chorioretinal dysplasia, microphthalmia, microcephaly, mental retardation
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7Academic Journal
المؤلفون: Cordewener, FW, Bos, RRM, Rozema, FR, Houtman, WA
المصدر: Cordewener , FW , Bos , RRM , Rozema , FR & Houtman , WA 1996 , ' Poly(L-lactide) implants for repair of human orbital floor defects : Clinical and magnetic resonance imaging evaluation of long-term results ' , Journal of Oral and Maxillofacial Surgery , vol. 54 , no. 1 , pp. 9-13 .
مصطلحات موضوعية: FOREIGN-BODY REACTIONS, BLOW-OUT FRACTURES, ZYGOMATIC FRACTURES, INTERNAL-FIXATION, TISSUE-RESPONSE, BONE-PLATES, SCREWS, MANAGEMENT, INJURIES, POLYMERS
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8Academic Journal
المؤلفون: KOOIJMAN, AC, KEMPEN, GIJM, CORNELISSEN, FW, VANHEUVELEN, MJG, VANDEWEGE, A, FRITSCHE, P, HOUTMAN, WA
المساهمون: Kooijman, AC, Looijestijn, PL, Welling, JA, VanDerWildt, GJ
المصدر: KOOIJMAN , AC , KEMPEN , GIJM , CORNELISSEN , FW , VANHEUVELEN , MJG , VANDEWEGE , A , FRITSCHE , P & HOUTMAN , WA 1994 , SCREENING OF VISUAL FUNCTION COMPARED WITH SELF-REPORT VISUAL DISABILITY . in AC Kooijman , PL Looijestijn , JA Welling & GJ VanDerWildt (eds) , LOW VISION . STUDIES IN HEALTH TECHNOLOGY AND INFORMATICS , vol. 11 , I O S PRESS , AMSTERDAM , pp. 11-14 , VISION 1993, the International Conference on Low Vision , Netherlands , 05/07/1993 .
Relation: https://research.rug.nl/en/publications/9ab90eea-d973-4643-b99e-f372ea5bab8a; urn:ISBN:90-5199-144-4
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9
المؤلفون: Hordijk, R, VandeLogt, F, Houtman, WA, VanEssen, AJ
المصدر: Genetic counseling, 7(2), 113-122
مصطلحات موضوعية: chorioretinal dysplasia, microphthalmia, microcephaly, mental retardation
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10Academic Journal
المؤلفون: DEKEIZER, RJW, OOSTERHUIS, JA, HOUTMAN, WA, DEWOLFFROUENDAAL, D
المصدر: DEKEIZER , RJW , OOSTERHUIS , JA , HOUTMAN , WA & DEWOLFFROUENDAAL , D 1993 , ' TAPIOCA MELANOMA OF THE IRIS ' , Annals of ophthalmology , vol. 25 , no. 5 , pp. 195-198 . ; ISSN:0003-4886
مصطلحات موضوعية: MALIGNANT-MELANOMA
الاتاحة: http://hdl.handle.net/11370/3555db5f-50dc-4306-95ba-71f7fb8d8b74
https://research.rug.nl/en/publications/tapioca-melanoma-of-the-iris(3555db5f-50dc-4306-95ba-71f7fb8d8b74).html -
11
المؤلفون: ENGLE, EC, MARONDEL, [No Value], HOUTMAN, WA, DEVRIES, B, LOEWENSTEIN, A, LAZAR, M, WARD, DC, KUCHERLAPATI, R, BEGGS, AH
المصدر: American Journal of Human Genetics, 57(5), 1086-1094. CELL PRESS
مصطلحات موضوعية: SEQUENCES, INSITU HYBRIDIZATION, DNA, CLONES
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12Academic Journal
المؤلفون: COENRAADS, PJ, WOEST, TE, BLANKSMA, LJ, HOUTMAN, WA
المصدر: COENRAADS , PJ , WOEST , TE , BLANKSMA , LJ & HOUTMAN , WA 1990 , ' CONTACT ALLERGY TO D-PENICILLAMINE ' , Contact Dermatitis , vol. 23 , no. 5 , pp. 371-372 .
مصطلحات موضوعية: ALLERGIC CONTACT DERMATITIS, ALLERGIC CONTACT CONJUNCTIVITIS, EYEDROPS, D-PENICILLAMINE, MEDICAMENTS, OPHTHALMOLOGY
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13Academic Journal
المؤلفون: TROELSTRA, A, RIJNEVELD, WJ, KOOIJMAN, AC, HOUTMAN, WA
المصدر: TROELSTRA , A , RIJNEVELD , WJ , KOOIJMAN , AC & HOUTMAN , WA 1988 , ' CORRELATION BETWEEN NMR SCANS OF EXTRAOCULAR-MUSCLES AND CLINICAL SYMPTOMS IN GRAVES OPHTHALMOPATHY ' , Documenta ophthalmologica , vol. 70 , no. 2-3 , pp. 243-249 .
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14Academic Journal
المؤلفون: HOUTMAN, WA, VANWEERDEN, TW, ROBINSON, PH, DEVRIES, B, HOOGENRAAD, TU
المصدر: HOUTMAN , WA , VANWEERDEN , TW , ROBINSON , PH , DEVRIES , B & HOOGENRAAD , TU 1986 , ' HEREDITARY CONGENITAL EXTERNAL OPHTHALMOPLEGIA ' , Ophthalmologica , vol. 193 , no. 4 , pp. 207-218 .
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15Academic Journal
المؤلفون: RIJNEVELD, WJ, JONGEBLOED, WL, WORST, JGF, HOUTMAN, WA
المصدر: RIJNEVELD , WJ , JONGEBLOED , WL , WORST , JGF & HOUTMAN , WA 1989 , ' COMPARISON OF THE REACTION OF THE CORNEA TO NYLON AND STAINLESS-STEEL SUTURES - AN ANIMAL STUDY ' , Documenta ophthalmologica , vol. 72 , no. 3-4 , pp. 297-307 . ; ISSN:0012-4486
الاتاحة: http://hdl.handle.net/11370/471f4804-8439-440c-8955-29dc838fb49f
https://research.rug.nl/en/publications/comparison-of-the-reaction-of-the-cornea-to-nylon-and-stainlesssteel-sutures--an-animal-study(471f4804-8439-440c-8955-29dc838fb49f).html -
16Academic Journal
المؤلفون: VANWEERDEN, TW, HOUTMAN, WA
المصدر: VANWEERDEN , TW & HOUTMAN , WA 1984 , ' MANIFEST LATENT NYSTAGMUS OF LATE ONSET - A CASE-REPORT ' , Ophthalmologica , vol. 188 , no. 3 , pp. 153-158 . ; ISSN:0030-3755
الاتاحة: http://hdl.handle.net/11370/78c900e6-d752-48da-8c0b-77c22d92acf6
https://research.rug.nl/en/publications/manifest-latent-nystagmus-of-late-onset--a-casereport(78c900e6-d752-48da-8c0b-77c22d92acf6).html -
17Academic Journal
المؤلفون: HOUTMAN, WA, ROZE, JH, SCHEPER, W
المصدر: HOUTMAN , WA , ROZE , JH & SCHEPER , W 1977 , ' VERTICAL MOTOR FUSION ' , Documenta ophthalmologica , vol. 44 , no. 1 , pp. 179-185 . ; ISSN:0012-4486
الاتاحة: http://hdl.handle.net/11370/061771fc-0786-4d36-9481-021e9460b937
https://research.rug.nl/en/publications/vertical-motor-fusion(061771fc-0786-4d36-9481-021e9460b937).html -
18
المؤلفون: Monte A. Del Monte, Berendina De Vries, Arnold London, Wai-Man Chan, Emin Cumhur Sener, Anat Loewenstein, Joseph L. Demer, Elizabeth C. Engle, Nakamichi Saito, Robert P. Cruse, Michael C. Brodsky, A. Nurten Akarsu, Roger H. Johnson, Mark S. Ruttum, Alina A. Zubcov, Alex V. Levin, Naomichi Matsumoto, Blaine L. Hart, Teresa de Berardinis, Lionel Kowal, Ravi Battu, Marlene C. Vogel, Michael O'Keefe, Thomas J. Carlow, Frank Hanisch, Banu T. Öztürk, Caroline Andrews, Robert D. Letson, Moshe Lazar, Eiichiro Uyama, Craig A. McKeown, James A. Katowitz, Scott M. Goldstein, Piergiorgio Franceschini, Richard M. Robb, Lisa Morris, Adriano Magli, Koki Yamada, Peter Roggenkäemper, Nicolas Krawiecki, Willem A. Houtman, John M. Shoffner, Anna Newlin, Elias I. Traboulsi, Irene Gottlob
المساهمون: Yamada, K, Andrews, C, Chan, Wm, Mckeown, Ca, Magli, A, DE BERARDINIS, Teresa, Loewenstein, A, Lazar, M, O'Keefe, M, Letson, R, London, A, Ruttum, M, Matsumoto, N, Saito, N, Morris, L, DEL MONTE, M, Johnson, Rh, Uyama, E, Houtman, Wa, DE VRIES, B, Carlow, Tj, Hart, Bl, Krawiecki, N, Shoffner, J, Vogel, Mc, Katowitz, J, Goldstein, Sm, Levin, Av, Sener, Ec, Ozturk, Bt, Akarsu, An, Brodsky, Mc, Hanisch, F, Cruse, Rp, Zubcov, Aa, Robb, Rm, Roggenkaemper, P, Gottlob, I, Kowal, L, Battu, R, Traboulsi, Ei, Franceschini, P, Newlin, A, Demer, Jl, Engle, E. C.
المصدر: Nature Genetics, 35(4), 318-321. Nature Publishing Group
مصطلحات موضوعية: Proband, Male, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, genetic structures, Genetic Linkage, Molecular Sequence Data, Kinesins, Nerve Tissue Proteins, Biology, REGION, Motor protein, Mutational hotspot, Congenital fibrosis of the extraocular muscles, MAPS, Genetics, medicine, Missense mutation, Humans, Amino Acid Sequence, Strabismus, Child, Ophthalmoplegia, Sequence Homology, Amino Acid, CHROMOSOME-12, REFINEMENT, Oculomotor nerve, Genetic Variation, EXTERNAL OPHTHALMOPLEGIA, medicine.disease, Fibrosis, eye diseases, Pedigree, Phenotype, Oculomotor Muscles, Mutation, Kinesin, Female
وصف الملف: STAMPA