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Items: 1 to 20 of 28

1.

Liver pathology and immunocytochemistry in congenital peroxisomal diseases: a review.

Roels F, Espeel M, De Craemer D.

J Inherit Metab Dis. 1991;14(6):853-75. Review.

PMID:
1779645
2.

Peroxisomal disorders: clinical characterization.

Monnens L, Heymans H.

J Inherit Metab Dis. 1987;10 Suppl 1:23-32. Review.

PMID:
2446046
3.

Peroxisomal disorders in neurology.

Wanders RJ, Heymans HS, Schutgens RB, Barth PG, van den Bosch H, Tager JM.

J Neurol Sci. 1988 Dec;88(1-3):1-39. Review.

PMID:
3066850
4.

New approaches in peroxisomal disorders.

Moser HW.

Dev Neurosci. 1987;9(1):1-18. Review.

PMID:
3297624
5.

[Peroxisomes and neurologic diseases].

Sereni C, Paturneau-Jouas M.

Rev Neurol (Paris). 1989;145(5):341-9. Review. French.

PMID:
2472665
6.

[Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers].

Molzer B, Stöckler S, Bernheimer H.

Wien Klin Wochenschr. 1992;104(21):665-70. Review. German.

PMID:
1282286
7.

Prenatal and perinatal diagnosis of peroxisomal disorders.

Schutgens RB, Schrakamp G, Wanders RJ, Heymans HS, Tager JM, van den Bosch H.

J Inherit Metab Dis. 1989;12 Suppl 1:118-34. Review.

PMID:
2509803
8.

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

Roels F, Espeel M, Poggi F, Mandel H, van Maldergem L, Saudubray JM.

Biochimie. 1993;75(3-4):281-92. Review.

PMID:
7685191
9.

Peroxisomal disorders: clinical commentary and future prospects.

Wilson GN, Holmes RD, Hajra AK.

Am J Med Genet. 1988 Jul;30(3):771-92. Review.

PMID:
2461077
10.

Clinical biochemistry of peroxisomal disorders.

Kaiser E, Kramar R.

Clin Chim Acta. 1988 Mar 31;173(1):57-80. Review.

PMID:
3289796
11.

Clinical approach to inherited peroxisomal disorders.

Poggi-Travert F, Fournier B, Poll-The BT, Saudubray JM.

J Inherit Metab Dis. 1995;18 Suppl 1:1-18. Review.

PMID:
9053544
12.

Peroxisomal disorders.

Moser HW, Bergin A, Cornblath D.

Biochem Cell Biol. 1991 Jul;69(7):463-74. Review.

PMID:
1724376
13.

Peroxisomal disorders. A review of a recently recognized group of clinical entities.

Talwar D, Swaiman KF.

Clin Pediatr (Phila). 1987 Oct;26(10):497-504. Review.

PMID:
2443295
14.

The peroxisome and the eye.

Folz SJ, Trobe JD.

Surv Ophthalmol. 1991 Mar-Apr;35(5):353-68. Review.

PMID:
1710072
15.

Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment.

Schutgens RB, Wanders RJ, Heymans HS, Schram AW, Tager JM, Schrakamp G, van den Bosch H.

J Inherit Metab Dis. 1987;10 Suppl 1:33-45. Review.

PMID:
3119940
16.

[Peroxisomal hereditary metabolic disorders].

Chandoga J, Petrovic R.

Cas Lek Cesk. 2001 Oct 25;140(21):651-7. Review. Slovak.

PMID:
11766453
17.

Disorders related to the metabolism of phytanic acid.

Stokke O, Skjeldal OH, Høie K.

Scand J Clin Lab Invest Suppl. 1986;184:3-10. Review.

PMID:
2438746
18.

[Peroxisomes--in search of their function in man].

Monnens L, Trijbels F, Govaerts L.

Tijdschr Kindergeneeskd. 1985 Aug;53(4):129-36. Review. Dutch.

PMID:
3909510
19.

Peroxisomal diseases.

Palosaari PM, Kilponen JM, Hiltunen JK.

Ann Med. 1992 Jun;24(3):163-6. Review.

PMID:
1627308
20.

Human peroxisomal disorders.

Depreter M, Espeel M, Roels F.

Microsc Res Tech. 2003 Jun 1;61(2):203-23. Review.

PMID:
12740827
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