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

Neuromuscular disorders : NMD, 2011-06, Vol.21 (6), p.420-427

2011

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

Neuromuscular disorders : NMD, 2010-11, Vol.20 (11), p.709-711

2010

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A 72-year-old woman with right frontal extra-axial mass

Brain pathology (Zurich, Switzerland), 2008-04, Vol.18 (2), p.279

2008

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

Neuromuscular disorders : NMD, 2013-05, Vol.23 (5), p.391-398

2013

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

Neuromuscular disorders : NMD, 2010-03, Vol.20 (3), p.166-173

2010

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Infantile onset myofibrillar myopathy due to recessive CRYAB mutations

Neuromuscular disorders : NMD, 2011-01, Vol.21 (1), p.37-40

2011

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CORRESPONDENCE: Reader Submitted Cases of the MonthEdited by Dr Ronald L. HamiltonOCTOBER 2007 CASE 1: A 72-YEAR-OLD WOMAN WITH RIGHT FRONTAL EXTRA-AXIAL MASS

Brain pathology (Zurich, Switzerland), 2008-04, Vol.18 (2), p.279-282

2008

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CORRESPONDENCE: Reader Submitted Cases of the Month Edited by Dr Ronald L. Hamilton OCTOBER 2007 CASE 1: A 72‐YEAR‐OLD WOMAN WITH RIGHT FRONTAL EXTRA‐AXIAL MASS

Brain pathology (Zurich, Switzerland), 2008-04, Vol.18 (2), p.279-282

2008

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Simultaneous Demonstration of Connective Tissue elastica and Fibrin by a Combined Verhoeff's Elastic-Martius-Scarlet-Blue Trichrome Stain

Biotechnic & histochemistry, 1984, Vol.59 (1), p.1-5

Buk, Stefan J. A.

1984

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

The Histochemical journal, 1986-10, Vol.18 (10), p.576-578

1986

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

The Histochemical journal, 1986-05, Vol.18 (5), p.228-232

1986

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A 72-year-old woman with right frontal extra-axial mass

Brain pathology (Zurich, Switzerland), 2008, Vol.18 (2), p.279-282

2008

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Business-NGO collaborations in Turkey: The bottom-of-the-pyramid paradigm

Base of the Pyramid Markets in Asia, 2020, p.69-91

1, 2020

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

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

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

A 72-year-old woman with right frontal extra-axial mass

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

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

Infantile onset myofibrillar myopathy due to recessive CRYAB mutations

CORRESPONDENCE: Reader Submitted Cases of the MonthEdited by Dr Ronald L. HamiltonOCTOBER 2007 CASE 1: A 72-YEAR-OLD WOMAN WITH RIGHT FRONTAL EXTRA-AXIAL MASS

CORRESPONDENCE: Reader Submitted Cases of the Month Edited by Dr Ronald L. Hamilton OCTOBER 2007 CASE 1: A 72‐YEAR‐OLD WOMAN WITH RIGHT FRONTAL EXTRA‐AXIAL MASS

Simultaneous Demonstration of Connective Tissue elastica and Fibrin by a Combined Verhoeff's Elastic-Martius-Scarlet-Blue Trichrome Stain

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

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

A 72-year-old woman with right frontal extra-axial mass

Business-NGO collaborations in Turkey: The bottom-of-the-pyramid paradigm

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