Topics
autosomal recessiveDisease
Hermansky-Pudlak syndromeDisease
oculocutaneous albinismDisease
plateletMilitary unit
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder which is characterised by the triad of oculocutaneous albinism, platelet dysfunction and accumulation of ceroidlike pigment in tissues
A 26-year-old Japanese woman was admitted with a 1-month history of diarrhea, a high fever for a few...
Hermansky-Pudlak syndrome (HPS) is a rare genetic disorder, the most common complication of which in...
SummaryHermansky-Pudlak syndrome (HPS) consists of oculocutaneous albinism, a platelet storage-pool ...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder which is characterised by the...
Hermansky-Pudlak syndrome is a rare syndrome characterized by bleeding diathesis due to platelet dys...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which results in oculocutane...
Abstract Background Hermansky-Pudlak syndrome (HPS) is a rare, genetically heterogeneous disorder th...
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive genetic disorder in which the proper funct...
Hermansky-Pudlak syndrome is a rare autosomal recessive multisystem disease, with oculocutneous albi...
Hermansky-Pudlak syndrome (HPS) is a rare form of syndromic oculocutaneous albinism caused by disord...
Hermansky-Pudlak syndrome (HPS) associates oculocutaneous albinism and systemic affections including...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder caused by defects in 10 human...
Objective. The aim of this paper is to report the case of a patient diagnosed with Hermansky-Pudlak ...
Griscelli syndrome (GS) was diagnosed in a 2-year-old patient with oculocutaneous albinism and immun...
Hermansky-Pudlak syndrome (HPS) is a heterogeneous disorder combining oculocutaneous albinism (OCA) ...
A 26-year-old Japanese woman was admitted with a 1-month history of diarrhea, a high fever for a few...
Hermansky-Pudlak syndrome (HPS) is a rare genetic disorder, the most common complication of which in...
SummaryHermansky-Pudlak syndrome (HPS) consists of oculocutaneous albinism, a platelet storage-pool ...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder which is characterised by the...
Hermansky-Pudlak syndrome is a rare syndrome characterized by bleeding diathesis due to platelet dys...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which results in oculocutane...
Abstract Background Hermansky-Pudlak syndrome (HPS) is a rare, genetically heterogeneous disorder th...
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive genetic disorder in which the proper funct...
Hermansky-Pudlak syndrome is a rare autosomal recessive multisystem disease, with oculocutneous albi...
Hermansky-Pudlak syndrome (HPS) is a rare form of syndromic oculocutaneous albinism caused by disord...
Hermansky-Pudlak syndrome (HPS) associates oculocutaneous albinism and systemic affections including...
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder caused by defects in 10 human...
Objective. The aim of this paper is to report the case of a patient diagnosed with Hermansky-Pudlak ...
Griscelli syndrome (GS) was diagnosed in a 2-year-old patient with oculocutaneous albinism and immun...
Hermansky-Pudlak syndrome (HPS) is a heterogeneous disorder combining oculocutaneous albinism (OCA) ...
A 26-year-old Japanese woman was admitted with a 1-month history of diarrhea, a high fever for a few...
Hermansky-Pudlak syndrome (HPS) is a rare genetic disorder, the most common complication of which in...
SummaryHermansky-Pudlak syndrome (HPS) consists of oculocutaneous albinism, a platelet storage-pool ...
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