Ghent University Academic Bibliography

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- Conference Paper
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RESOLUTION OF THE MOLECULAR DEFECT IN A PATIENT WITH PEROXISOMAL MOSAICISM IN THE LIVER USING A NEW MEHTOD

J GOOTJES, P MOOIJER, M MANDEL, Frank Roels (UGent) , H WATERHAM and R WANDERS

(2003) JOURNAL OF INHERITED METABOLIC DISEASE. 26(Suppl. 2). p.177-7
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- Journal Article
- A1
Peroxisome mosaics

Frank Roels (UGent) , Jean-Marie Saudubray, Marisa Giros, Hanna Mandel, François Eyskens, Nieves Saracibar, Begona Atares Pueyo, Jose M Prats, Betty De Prest, Katleen De Preter (UGent) , et al.

(2003) Advances in Experimental Medicine and Biology. 544. p.97-106
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Peroxisome mosaics in patients : modulation of gene expression?

Frank Roels (UGent) , Hanna Mandel, Marisa Giros, François Eyskens, Mercedes Pineda, Jeannette Gootjes, Marc Espeel (UGent) , Bwee Tien Poll-The and Jean-Marie Saudubray

(2003) Jaarboek Nederlandse Vereniging voor Microscopie. 2003. p.37-39
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- Journal Article
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Resolution of the molecular defect in a patient with peroxisomal mosaicism in the liver

J GOOTJES, H MANDEL, PAW MOOIJER, Frank Roels (UGent) , HR WATERHAM and RJA WANDERS

(2003) PEROXISOMAL DISORDERS AND REGULATION OF GENES. 544. p.107-111
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- C3
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Peroxisome mosaics revisited : follow-up of 10 patients

Frank Roels (UGent) , Hanna Mandel, Marisa Giros, François Eyskens, Mercedes Pineda, Jeannette Gootjes, Ronald JA Wanders, Marc Espeel (UGent) , Bwee Tien Poll-The and Jean-Marie Saudubray

(2003) JOURNAL OF INHERITED METABOLIC DISEASE. 26(suppl. 2). p.181-181
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- Journal Article
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A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.

A RAAS-ROTHSCHILD, R WANDERS, P MOOIJER, J GOOTJES, HR WATERHAM, A GUTMAN, Y SUZUKI, N SHIMOZAWA, N KONDO, G ESHEL, et al.

(2002) AMERICAN JOURNAL OF HUMAN GENETICS. 70(4). p.1062-1068

Academic Bibliography

RESOLUTION OF THE MOLECULAR DEFECT IN A PATIENT WITH PEROXISOMAL MOSAICISM IN THE LIVER USING A NEW MEHTOD

Peroxisome mosaics

Peroxisome mosaics in patients : modulation of gene expression?

Resolution of the molecular defect in a patient with peroxisomal mosaicism in the liver

Peroxisome mosaics revisited : follow-up of 10 patients

A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.

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