Malin JP - Search Results

1

A missense point mutation (Ser515Phe) in the adrenoleukodystrophy gene in a family with adrenomyeloneuropathy: a clinical, biochemical, and genetic study.

Vorgerd M, Fuchs S, Tegenthoff M, Malin JP. Vorgerd M, et al. Among authors: malin jp. J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):229-31. doi: 10.1136/jnnp.58.2.229. J Neurol Neurosurg Psychiatry. 1995. PMID: 7876858 Free PMC article.

2

Mutation analysis in myophosphorylase deficiency (McArdle's disease).

Vorgerd M, Kubisch C, Burwinkel B, Reichmann H, Mortier W, Tettenborn B, Pongratz D, Lindemuth R, Tegenthoff M, Malin JP, Kilimann MW. Vorgerd M, et al. Among authors: malin jp. Ann Neurol. 1998 Mar;43(3):326-31. doi: 10.1002/ana.410430310. Ann Neurol. 1998. PMID: 9506549

3

[Adrenoleukodystrophy and adrenomyeloneuropathy. Clinical biochemical and molecular genetic findings].

Vorgerd M, Benkmann HG, Tegenthoff M, Gal A, Malin JP. Vorgerd M, et al. Among authors: malin jp. Nervenarzt. 1998 Feb;69(2):174-9. doi: 10.1007/s001150050257. Nervenarzt. 1998. PMID: 9551465 German.

4

Novel missense mutations in the glycogen-branching enzyme gene in adult polyglucosan body disease.

Ziemssen F, Sindern E, Schröder JM, Shin YS, Zange J, Kilimann MW, Malin JP, Vorgerd M. Ziemssen F, et al. Among authors: malin jp. Ann Neurol. 2000 Apr;47(4):536-40. Ann Neurol. 2000. PMID: 10762170

5

Spinal MRI in progressive myeloneuropathy associated with vitamin E deficiency.

Vorgerd M, Tegenthoff M, Kühne D, Malin JP. Vorgerd M, et al. Among authors: malin jp. Neuroradiology. 1996 May;38 Suppl 1:S111-3. doi: 10.1007/BF02278134. Neuroradiology. 1996. PMID: 8811695

6

Muscle phosphofructokinase deficiency in two generations.

Vorgerd M, Karitzky J, Ristow M, Van Schaftingen E, Tegenthoff M, Jerusalem F, Malin JP. Vorgerd M, et al. Among authors: malin jp. J Neurol Sci. 1996 Sep 15;141(1-2):95-9. doi: 10.1016/0022-510x(96)00131-1. J Neurol Sci. 1996. PMID: 8880699

7

Phenotypic variability in rippling muscle disease.

Vorgerd M, Bolz H, Patzold T, Kubisch C, Malin JP, Mortier W. Vorgerd M, et al. Among authors: malin jp. Neurology. 1999 Apr 22;52(7):1453-9. doi: 10.1212/wnl.52.7.1453. Neurology. 1999. PMID: 10227634

8

Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patients.

Vorgerd M, Burwinkel B, Reichmann H, Malin JP, Kilimann MW. Vorgerd M, et al. Among authors: malin jp. Neurogenetics. 1998 Mar;1(3):205-11. doi: 10.1007/s100480050030. Neurogenetics. 1998. PMID: 10737124

9

Creatine therapy in myophosphorylase deficiency (McArdle disease): a placebo-controlled crossover trial.

Vorgerd M, Grehl T, Jager M, Muller K, Freitag G, Patzold T, Bruns N, Fabian K, Tegenthoff M, Mortier W, Luttmann A, Zange J, Malin JP. Vorgerd M, et al. Among authors: malin jp. Arch Neurol. 2000 Jul;57(7):956-63. doi: 10.1001/archneur.57.7.956. Arch Neurol. 2000. PMID: 10891977 Clinical Trial.

10

Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophies.

Vorgerd M, Gencik M, Mortier J, Epplen JT, Malin JP, Mortier W. Vorgerd M, et al. Among authors: malin jp. Muscle Nerve. 2001 Mar;24(3):421-4. doi: 10.1002/1097-4598(200103)24:3<421::aid-mus1016>3.0.co;2-r. Muscle Nerve. 2001. PMID: 11353430

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