367 results on '"Pas, Hendri H."'
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52. The IgG “Lupus-Band” Deposition Pattern of Pemphigus Erythematosus: Association With the Desmoglein 1 Ectodomain as Revealed by 3 Cases
53. The effectiveness of rituximab in pemphigus and the benefit of additional maintenance infusions: Daily practice data from a retrospective study
54. Immunoglobulin M bullous pemphigoid: An enigma
55. Hyperkeratotic hand eczema: Eczema or not?
56. Abundance of the Long Pentraxin PTX3 at Sites of Leukocytoclastic Lesions in Patients With Small-Vessel Vasculitis
57. Revertant mosaicism in epidermolysis bullosa caused by mitotic gene conversion
58. Anti-epiligrin cicatricial pemphigoid and epidermolysis bullosa acquisita: Differentiation by use of indirect immunofluorescence microscopy
59. Deletion of a Cytoplasmic Domain of Integrin β4 Causes Epidermolysis Bullosa Simplex
60. IgA-mediated epidermolysis bullosa acquisita: Two cases and review of the literature
61. Transition of pemphigus vulgaris into pemphigus foliaceus confirmed by antidesmoglein ELISA profile
62. Partial Revertant Mosaicism of Keratin 14 in a Patient with Recessive Epidermolysis Bullosa Simplex1
63. Inflammatory Variant of Epidermolysis Bullosa Acquisita With IgG Autoantibodies Against Type VII Collagen and Laminin α3
64. The expression pattern of N‐acetyltransferase 1 in healthy human skin.
65. Type XVII Collagen (BP180) and LAD-1 are Present as Separate Trimeric Complexes
66. Prevalence of Pemphigoid as a Potentially Unrecognized Cause of Pruritus in Nursing Home Residents
67. Endocytosis of IgG, Desmoglein 1, and Plakoglobin in Pemphigus Foliaceus Patient Skin
68. Reply to: “Pruritus with pemphigoid autoantibodies is the tip of an iceberg”
69. Nonbullous pemphigoid: Insights in clinical and diagnostic findings, treatment responses, and prognosis
70. Assessment of Diagnostic Strategy for Early Recognition of Bullous and Nonbullous Variants of Pemphigoid
71. Biochemical detection of antigens recognized by bullous dermatoses autoantibodies: SM6–8
72. IGA- and IGG-epitopes in subepidermal immunobuilous dermatoses: S10–3
73. LAD-1 Is Absent in a Subset of Junctional Epidermolysis Bullosa Patients
74. Bullous Pemphigoid and Linear IgA Dermatosis Sera Recognize a Similar 120-kDa Keratinocyte Collagenous Glycoprotein with Antigenic Cross-Reactivity to BP180
75. Nuclear Proteins and Apoptotic Bodies Are Found in the Lupus Band of Patients with Cutaneous Lupus Erythematosus
76. Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
77. A PLEC Isoform Identified in Skin, Muscle, and Heart
78. Effects of Keratin 14 Ablation on the Clinical and Cellular Phenotype in a Kindred with Recessive Epidermolysis Bullosa Simplex
79. Bullous Pemphigoid and Epidermolysis Bullosa Acquisita: Differentiation by Fluorescence Overlay Antigen Mapping
80. 180-kD Bullous Pemphigoid Antigen (BP180) Is Deficient in Generalized Atrophic Benign Epidermolysis Bullosa
81. Truncated Type XVII Collagen Expression in a Patient with Non-Herlitz Junctional Epidermolysis Bullosa Caused by a Homozygous Splice-Site Mutation
82. Immunoblot assay in differential diagnosis of autoimmune blistering skin diseases
83. Particle Bombardment of Ex Vivo Skin to Deliver DNA and Express Proteins
84. Keratinocyte Binding Assay Identifies Anti-Desmosomal Pemphigus Antibodies Where Other Tests Are Negative
85. Serration pattern analysis for differentiating epidermolysis bullosa acquisita from other pemphigoid diseases
86. Type VII Collagen in the Human Accommodation System: Expression in Ciliary Body, Zonules, and Lens Capsule
87. Whole-Genome Expression Profiling in Skin Reveals SYK As a Key Regulator of Inflammation in Experimental Epidermolysis Bullosa Acquisita
88. Human retinal Müller cells synthesize collagens of the vitreous and vitreoretinal interface in vitro
89. Conditional depletion of mast cells has no impact on the severity of experimental epidermolysis bullosa acquisita
90. Direct Immunofluorescence of Mechanobullous Epidermolysis Bullosa Acquisita, Porphyria Cutanea Tarda and Pseudoporphyria.
91. The smallest resonance energy transfer acceptor for tryptophan
92. Carriers with functional null mutations in LAMA3 have localized enamel abnormalities due to haploinsufficiency
93. PDE4 Inhibition as Potential Treatment of Epidermolysis Bullosa Acquisita
94. Laboratory Diagnosis and Clinical Profile of Anti-p200 Pemphigoid
95. Bullous Pemphigoid With a Dual Pattern of Glomerular Immune Complex Disease
96. Epiplakin Is a Paraneoplastic Pemphigus Autoantigen and Related to Bronchiolitis Obliterans in Japanese Patients
97. Inflammatory Variant of Epidermolysis Bullosa Acquisita With IgG Autoantibodies Against Type VII Collagen and Laminin [alpha]3
98. Type VII Collagen Expression in the Human Vitreoretinal Interface, Corpora Amylacea and Inner Retinal Layers
99. Large-Scale Electron Microscopy Maps of Patient Skin and Mucosa Provide Insight into Pathogenesis of Blistering Diseases
100. Autoantibodies to Multiple Epitopes on the Non-Collagenous-1 Domain of Type VII Collagen Induce Blisters
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