<p>Representative whole-mount electron micrographs of platelets from a patient with Hermansky-Pudlak syndrome (A) and normal platelets (B) are shown (bar = 1 micrometer). Normal platelets contain delta granules (arrows), and platelets from patients with HPS are devoid of delta granules. Representative computed tomography scan of the chest from one patient with Hermansky-Pudlak syndrome pulmonary fibrosis showing diffuse bilateral parenchymal fibrosis with honeycombing and loss of lung volume (C) and from another patient with cystic lung destruction and upper lobe predominance of disease (D).</p
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder which is characterised by the...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder caused by defects in 10 human...
Hermansky-Pudlak syndrome (HPS) is a heterogeneous disorder combining oculocutaneous albinism (OCA) ...
Hermansky-Pudlak syndrome (HPS) is a disorder of lysosome-related organelle biogenesis that displays...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder characterized by oculocutaneo...
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive genetic disorder in which the proper funct...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which results in oculocutane...
Objective. The aim of this paper is to report the case of a patient diagnosed with Hermansky-Pudlak ...
Introduction: Platelet storage pool diseases (SPD) are a heterogeneous group of bleeding disorders a...
PubMedID: 24284295Hermansky-Pudlak Syndrome (HPS) is a rare autosomal recessive disorder presenting ...
Figure S4. CT scan of subject 4. CT Scan with patchy distribution of ground glass opacity throughout...
Background: Hermansky-Pudlak syndrome (HPS) is a rare inherited platelet disorder characterized by b...
Hermansky-Pudlak syndrome (HPS) is a rare form of syndromic oculocutaneous albinism caused by disord...
Hermansky-Pudlak syndrome (HPS) is a rare genetic disorder, the most common complication of which in...
One thousand and eighty patients, having prolonged bleeding times, frequent epistaxis, menorrhagia o...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder which is characterised by the...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder caused by defects in 10 human...
Hermansky-Pudlak syndrome (HPS) is a heterogeneous disorder combining oculocutaneous albinism (OCA) ...
Hermansky-Pudlak syndrome (HPS) is a disorder of lysosome-related organelle biogenesis that displays...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder characterized by oculocutaneo...
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive genetic disorder in which the proper funct...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which results in oculocutane...
Objective. The aim of this paper is to report the case of a patient diagnosed with Hermansky-Pudlak ...
Introduction: Platelet storage pool diseases (SPD) are a heterogeneous group of bleeding disorders a...
PubMedID: 24284295Hermansky-Pudlak Syndrome (HPS) is a rare autosomal recessive disorder presenting ...
Figure S4. CT scan of subject 4. CT Scan with patchy distribution of ground glass opacity throughout...
Background: Hermansky-Pudlak syndrome (HPS) is a rare inherited platelet disorder characterized by b...
Hermansky-Pudlak syndrome (HPS) is a rare form of syndromic oculocutaneous albinism caused by disord...
Hermansky-Pudlak syndrome (HPS) is a rare genetic disorder, the most common complication of which in...
One thousand and eighty patients, having prolonged bleeding times, frequent epistaxis, menorrhagia o...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder which is characterised by the...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder caused by defects in 10 human...
Hermansky-Pudlak syndrome (HPS) is a heterogeneous disorder combining oculocutaneous albinism (OCA) ...