Equivalent currents associated with morning-sector geomagnetic Pc5 pulsations during auroral substorms
Kauristie, K., Uspensky, M. V., Kleimenova, N. G., Kozyreva, O. V., Van De Kamp, M. M. J. L., Dubyagin, S. V., Massetti, S.
Published in Annales geophysicae (1988) (07.04.2016)
Published in Annales geophysicae (1988) (07.04.2016)
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Journal Article
Clinical features and X-inactivation in females heterozygous for creatine transporter defect
van de Kamp, JM, Mancini, GMS, Pouwels, PJW, Betsalel, OT, van Dooren, SJM, de Koning, I, Steenweg, ME, Jakobs, C, van der Knaap, MS, Salomons, GS
Published in Clinical genetics (01.03.2011)
Published in Clinical genetics (01.03.2011)
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Journal Article
The etiological evaluation of sensorineural hearing loss in children
van Beeck Calkoen, E. A., Engel, M. S. D., van de Kamp, J. M., Yntema, H. G., Goverts, S.T., Mulder, M.F., Merkus, P., Hensen, E. F.
Published in European journal of pediatrics (01.08.2019)
Published in European journal of pediatrics (01.08.2019)
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Journal Article
Spectra of equatorial total electron content derived from GPS signals
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Journal Article
Conference Proceeding
Body‐and movement‐oriented interventions for posttraumatic stress disorder: An updated systematic review and meta‐analysis
van de Kamp, Minke M., Scheffers, Mia, Emck, Claudia, Fokker, Ties J., Hatzmann, Janneke, Cuijpers, Pim, Beek, Peter J.
Published in Journal of traumatic stress (01.10.2023)
Published in Journal of traumatic stress (01.10.2023)
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Journal Article
X-linked creatine transporter deficiency: clinical aspects and pathophysiology
van de Kamp, Jiddeke M., Mancini, Grazia M., Salomons, Gajja S.
Published in Journal of inherited metabolic disease (01.09.2014)
Published in Journal of inherited metabolic disease (01.09.2014)
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Journal Article
The role of the clinician in the multi-omics era: are you ready?
van Karnebeek, Clara D. M., Wortmann, Saskia B., Tarailo-Graovac, Maja, Langeveld, Mirjam, Ferreira, Carlos R., van de Kamp, Jiddeke M., Hollak, Carla E., Wasserman, Wyeth W., Waterham, Hans R., Wevers, Ron A., Haack, Tobias B., Wanders, Ronald J.A., Boycott, Kym M.
Published in Journal of inherited metabolic disease (01.05.2018)
Published in Journal of inherited metabolic disease (01.05.2018)
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Journal Article
SLC26A1 is a major determinant of sulfate homeostasis in humans
Pfau, Anja, López-Cayuqueo, Karen I, Scherer, Nora, Wuttke, Matthias, Wernstedt, Annekatrin, González Fassrainer, Daniela, Smith, Desiree Ec, van de Kamp, Jiddeke M, Ziegeler, Katharina, Eckardt, Kai-Uwe, Luft, Friedrich C, Aronson, Peter S, Köttgen, Anna, Jentsch, Thomas J, Knauf, Felix
Published in The Journal of clinical investigation (01.02.2023)
Published in The Journal of clinical investigation (01.02.2023)
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Journal Article
The first case of fatal familial insomnia (FFI) in the Netherlands: a patient from Egyptian descent with concurrent four repeat tau deposits
Jansen, C., Parchi, P., Jelles, B., Gouw, A. A., Beunders, G., van Spaendonk, R. M. L., van de Kamp, J. M., Lemstra, A. W., Capellari, S., Rozemuller, A. J. M.
Published in Neuropathology and applied neurobiology (01.08.2011)
Published in Neuropathology and applied neurobiology (01.08.2011)
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Journal Article
Clinical and genetic spectrum of Sanfilippo type C (MPS IIIC) disease in The Netherlands
Ruijter, G.J.G., Valstar, M.J., van de Kamp, J.M., van der Helm, R.M., Durand, S., van Diggelen, O.P., Wevers, R.A., Poorthuis, B.J., Pshezhetsky, A.V., Wijburg, F.A.
Published in Molecular genetics and metabolism (01.02.2008)
Published in Molecular genetics and metabolism (01.02.2008)
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Journal Article
Biallelic variants in the SLC13A1 sulfate transporter gene cause hyposulfatemia with a mild spondylo‐epi‐metaphyseal dysplasia
Kamp, Jiddeke M., Bökenkamp, Arend, Smith, Desiree E. C., Wamelink, Mirjam M. C., Jansen, Erwin E. W., Struys, Eduard A., Waisfisz, Quinten, Verkleij, Marieke, Hartmann, Michaela F., Wang, Rong, Wudy, Stefan A., Paganini, Chiara, Rossi, Antonio, Finken, Martijn J. J.
Published in Clinical genetics (01.01.2023)
Published in Clinical genetics (01.01.2023)
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Journal Article
Clinical, neuroradiological, and biochemical features of SLC35A2‐CDG patients
Vals, Mari‐Anne, Ashikov, Angel, Ilves, Pilvi, Loorits, Dagmar, Zeng, Qiang, Barone, Rita, Huijben, Karin, Sykut‐Cegielska, Jolanta, Diogo, Luísa, Elias, Abdallah F., Greenwood, Robert S., Grunewald, Stephanie, van Hasselt, Peter M., van de Kamp, Jiddeke M., Mancini, Grazia, Okninska, Agnieszka, Pajusalu, Sander, Rudd, Pauline M., Rustad, Cecilie F., Salvarinova, Ramona, de Vries, Bert B.A., Wolf, Nicole I., Ng, Bobby G., Freeze, Hudson H., Lefeber, Dirk J., Õunap, Katrin
Published in Journal of inherited metabolic disease (01.05.2019)
Published in Journal of inherited metabolic disease (01.05.2019)
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Journal Article
KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia
Pennings, Maartje, Schouten, Meyke I, van Gaalen, Judith, Meijer, Rowdy P P, de Bot, Susanne T, Kriek, Marjolein, Saris, Christiaan G J, van den Berg, Leonard H, van Es, Michael A, Zuidgeest, Dick M H, Elting, Mariet W, van de Kamp, Jiddeke M, van Spaendonck-Zwarts, Karin Y, Die-Smulders, Christine de, Brilstra, Eva H, Verschuuren, Corien C, de Vries, Bert B A, Bruijn, Jacques, Sofou, Kalliopi, Duijkers, Floor A, Jaeger, B, Schieving, Jolanda H, van de Warrenburg, Bart P, Kamsteeg, Erik-Jan
Published in European journal of human genetics : EJHG (01.01.2020)
Published in European journal of human genetics : EJHG (01.01.2020)
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Journal Article
Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patients
Sapp, Julie C., Turner, Joyce T., van de Kamp, Jiddeke M., van Dijk, Fleur S., Lowry, R. Brian, Biesecker, Leslie G.
Published in American journal of medical genetics. Part A (15.12.2007)
Published in American journal of medical genetics. Part A (15.12.2007)
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Journal Article