Van Maldergem L - Search Results

1

Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation.

Van Maldergem L, Espeel M, Wanders RJ, Roels F, Gerard P, Scalais E, Mannaerts GP, Casteels M, Gillerot Y. Van Maldergem L, et al. Neuromuscul Disord. 1992;2(3):217-24. doi: 10.1016/0960-8966(92)90009-u. Neuromuscul Disord. 1992. PMID: 1483048

2

Peroxisomal localization of the immunoreactive beta-oxidation enzymes in a neonate with a beta-oxidation defect. Pathological observations in liver, adrenal cortex and kidney.

Espeel M, Roels F, Van Maldergem L, De Craemer D, Dacremont G, Wanders RJ, Hashimoto T. Espeel M, et al. Among authors: van maldergem l. Virchows Arch A Pathol Anat Histopathol. 1991;419(4):301-8. doi: 10.1007/BF01606521. Virchows Arch A Pathol Anat Histopathol. 1991. PMID: 1949612

3

X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus.

Van Maldergem L, Espeel M, Roels F, Petit C, Dacremont G, Wanders RJ, Verloes A, Gillerot Y. Van Maldergem L, et al. Hum Genet. 1991 Oct;87(6):661-4. doi: 10.1007/BF00201721. Hum Genet. 1991. PMID: 1937466

4

Human liver pathology in peroxisomal diseases: a review including novel data.

Roels F, Espeel M, Poggi F, Mandel H, van Maldergem L, Saudubray JM. Roels F, et al. Among authors: van maldergem l. Biochimie. 1993;75(3-4):281-92. doi: 10.1016/0300-9084(93)90088-a. Biochimie. 1993. PMID: 7685191 Review.

5

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings.

Van Maldergem L, Tuerlinckx D, Wanders RJ, Vianey-Saban C, Van Hoof F, Martin JJ, Fourneau C, Gillerot Y, Bachy A. Van Maldergem L, et al. Among authors: van hoof f. Eur J Pediatr. 2000 Jan-Feb;159(1-2):108-12. doi: 10.1007/s004310050022. Eur J Pediatr. 2000. PMID: 10653342

6

Orthotopic liver transplantation from a living-related donor in an infant with a peroxisome biogenesis defect of the infantile Refsum disease type.

Van Maldergem L, Moser AB, Vincent MF, Roland D, Reding R, Otte JB, Wanders RJ, Sokal E. Van Maldergem L, et al. J Inherit Metab Dis. 2005;28(4):593-600. doi: 10.1007/s10545-005-0593-9. J Inherit Metab Dis. 2005. PMID: 15902563

7

Morphological features of a case of retinoic acid embryopathy.

Van Maldergem L, Jauniaux E, Gillerot Y. Van Maldergem L, et al. Prenat Diagn. 1992 Aug;12(8):699-701. doi: 10.1002/pd.1970120812. Prenat Diagn. 1992. PMID: 1438063

8

Hepatic ultrastructure in congenital total lipodystrophy with special reference to peroxisomes.

de Craemer D, Van Maldergem L, Roels F. de Craemer D, et al. Among authors: van maldergem l. Ultrastruct Pathol. 1992 May-Jun;16(3):307-16. doi: 10.3109/01913129209061360. Ultrastruct Pathol. 1992. PMID: 1585496

9

Genetic causes of hydrops fetalis.

Van Maldergem L, Jauniaux E, Fourneau C, Gillerot Y. Van Maldergem L, et al. Pediatrics. 1992 Jan;89(1):81-6. Pediatrics. 1992. PMID: 1728027

10

Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders.

Espeel M, Roels F, Giros M, Mandel H, Peltier A, Poggi F, Poll-The BT, Smeitink JA, Van Maldergem L, Santos MJ. Espeel M, et al. Among authors: van maldergem l. Eur J Cell Biol. 1995 Aug;67(4):319-27. Eur J Cell Biol. 1995. PMID: 8521871

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