S. Buk

发表

King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene

D. Baralle, F. Muntoni, S. Al-Sarraj, 2011, Neuromuscular Disorders.

PERLS‘ FERROCYANIDE TEST FOR IRON IN THE DIAGNOSIS OF VASCULITIC NEUROPATHY

C. W. Adams, R. Hughes, R. Hughes, 1989, Neuropathology and applied neurobiology.

Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectin

S. Al-Sarraj, J. McGrath, H. Jungbluth, 2010, Neuromuscular Disorders.

Periodate oxidation of glycolipids: A borohydride-periodate-Schiff method for ganglioside demonstration in tissue sections

S. Buk, O. B. Bayliss High, 1986, The Histochemical Journal.

Infantile onset myofibrillar myopathy due to recessive CRYAB mutations

K. Bushby, S. Al-Sarraj, M. Irving, 2011, Neuromuscular Disorders.

Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene

F. Muntoni, S. Al-Sarraj, Haiyan Zhou, 2010, Neuromuscular Disorders.

Simultaneous demonstration of connective tissue elastica and fibrin by a combined Verhoeff's elastic-Martius-scarlet-blue trichrome stain.

S. Buk, 1984, Stain technology.

An inter-observer and intra-observer variability study on the diagnosis of lymph node biopsy specimens.

W. Gregory, P. Hall, D. Levison, 1992, European journal of cancer.

Smooth muscle, leiomyomas and atherosclerosis.

C. W. Adams, Y. Abdulla, S. Buk, 1984, Atherosclerosis.

Inflammatory vasculitis in multiple sclerosis

R. Poston, S. Buk, H. Vipond, 1985, Journal of the Neurological Sciences.

Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene

T. Jacques, Amanda J Murphy, N. Dlamini, 2013, Neuromuscular Disorders.

Histochemical staining of sulphated and non-sulphated sialomucin in intestinal epithelium: Practical difficulties associated with the KOH—AB 1.0—PAPS method

M. Filipe, S. Buk, 1986, The Histochemical Journal.

Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy

E. Bertini, M. Simpson, H. Goebel, 2012, Nature Genetics.

Pathology, histochemistry and immunocytochemistry of lesions in acute multiple sclerosis

R. Poston, S. Buk, C. Adams, 1989, Journal of the Neurological Sciences.

Fat necrosis presenting as obscure abdominal mass: birefringent saponified fatty acid crystalloids as a clue to diagnosis.

D. Levison, K. Brady, S. Buk, 1994, Journal of Clinical Pathology.

King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene

D. Baralle, F. Muntoni, S. Al-Sarraj, 2011, Neuromuscular Disorders.

Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene

F. Muntoni, S. Al-Sarraj, Haiyan Zhou, 2010, Neuromuscular Disorders.