knobloch | Knobloch Strings

Keyword	CPC	PCC	Volume	Score	Length of keyword
knobloch	0.23	0.4	3279	16	8

Keyword	CPC	PCC	Volume	Score
knobloch	1.42	0.4	4837	9
knobloch syndrome	1.26	0.7	9654	67
knobloch strings	0.84	0.2	805	23
knobloch's greenhouse	0.35	1	868	69
knobloch jagd	1.25	0.4	6821	57
knobloch insurance	0.01	0.6	5250	69
knoblochova	1.58	0.5	3274	31
knobloch krefeld	1.15	0.2	6559	79
knobloch charlotte	1.13	0.1	3100	97
knobloch glasses	1.01	0.3	8536	51
knobloch autor	0.04	0.6	6495	88
knobloch shooting glasses	1.49	0.5	589	35
knobloch foundation	0.38	0.9	427	91
knobloch briefkastenanlagen	0.81	0.1	7872	66
knobloch family foundation	0.99	0.3	4361	34
knobloch gmbh	1.36	0.9	8993	32
knobloch sportwagen	1.44	0.1	7457	66
knobloch mailboxes	1.22	0.7	292	97
knobloch und knebel northeim	1.99	0.4	7774	18
knobloch classical guitar strings	0.44	0.7	9126	29
knobloch plumbing	1.97	0.3	5165	75
knobloch rhauderfehn	0.26	0.7	1919	97
knobloch schiessbrillen	1.48	0.6	7378	85
knobloch guitar strings	1.01	0.9	9082	66

Search Results related to knobloch on Search Engine

Knobloch Strings | Guitar Strings
knoblochstrings.com

https://www.knoblochstrings.com/

WEBKnobloch Strings creates handmade premium guitar strings. Created by musicians for musicians. We strive for comfort, good intonation and versatility in making our products.

DA: 59 PA: 11 MOZ Rank: 11

Knobloch syndrome - About the Disease - Genetic and Rare …
nih.gov

https://rarediseases.info.nih.gov/diseases/380/knobloch-syndrome/

WEBKnobloch syndrome follows an autosomal recessive pattern of inheritance. Knobloch syndrome is characterized by severe vision problems and skull defects. The most common features include extreme nearsightedness (high myopia), recurrent retinal detachment, and occipital encephalocele.

DA: 37 PA: 85 MOZ Rank: 54

Knobloch syndrome - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Knobloch_syndrome

WEBKnobloch syndrome is a rare genetic disorder presenting severe eyesight problems and often a defect in the skull. It was named after the ophthalmologist William Hunter Knobloch (1926–2005), who first described the syndrome in 1971. A usual occurrence is a degeneration of the vitreous humour and the retina, two components of the eye.

DA: 76 PA: 7 MOZ Rank: 99

Knobloch Syndrome - EyeWiki
aao.org

https://eyewiki.aao.org/Knobloch_Syndrome

WEBFirst described by Knobloch and Layer in 1971, Knobloch syndrome is a rare recessively inherited disorder characterized by high myopia, vitreoretinal degeneration and occipital skull defects, with a high degree of phenotypic variability.

DA: 83 PA: 6 MOZ Rank: 75

Knobloch syndrome: MedlinePlus Genetics
medlineplus.gov

https://medlineplus.gov/genetics/condition/knobloch-syndrome/

WEBDescription. Knobloch syndrome is a rare condition characterized by severe vision problems and a skull defect. A characteristic feature of Knobloch syndrome is extreme nearsightedness (high myopia ). In addition, several other eye abnormalities are common in people with this condition.

DA: 35 PA: 64 MOZ Rank: 58

GARD Rare Disease Information - Knobloch syndrome - National
rarediseases.org

https://rarediseases.org/gard-rare-disease/knobloch-syndrome/

WEBDisease Overview. Knobloch syndrome is characterized by severe vision problems and skull defects. [12388] The most common features include extreme nearsightedness (high myopia), recurrent retinal detachment, and occipital encephalocele . [12388] [2209] There are three types of Knobloch syndrome, which can be distinguished by the underlying ...

DA: 86 PA: 13 MOZ Rank: 29

Knobloch syndrome - Resources and Support - Genetic and Rare …
nih.gov

https://rarediseases.info.nih.gov/diseases/380/knobloch-syndrome/living/

WEBKnobloch syndrome. Other Names: . Knobloch-Layer syndrome; Retinal detachment-occipital encephalocele syndromeKnobloch-Layer syndrome; Retinal detachment-occipital encephalocele syndrome. Read More . Read Less . About the Disease . Getting a Diagnosis . Resources and Support . Discover Resources. Patient Resources. Caregiver …

DA: 77 PA: 99 MOZ Rank: 10

Three cases of molecularly confirmed Knobloch syndrome
tandfonline.com

https://www.tandfonline.com/doi/full/10.1080/13816810.2020.1737948

WEBMar 17, 2020 · Background: Knobloch syndrome (OMIM 267750) is a rare autosomal recessive disorder due to genetic defects in the COL18A1 gene. The triad of high myopia, occipital defect, vitreoretinal degeneration has been described as …

DA: 71 PA: 29 MOZ Rank: 19

Knobloch syndrome - Getting a Diagnosis - Genetic and Rare …
nih.gov

https://rarediseases.info.nih.gov/diseases/380/knobloch-syndrome/diagnosis/

WEBKnobloch syndrome. Other Names: . Knobloch-Layer syndrome; Retinal detachment-occipital encephalocele syndromeKnobloch-Layer syndrome; Retinal detachment-occipital encephalocele syndrome. Read More . Read Less . About the Disease . Getting a Diagnosis . Resources and Support . Diagnostic Journey. Your Diagnostic Team. Rare …

DA: 8 PA: 72 MOZ Rank: 51

Knobloch Syndrome 1 | Hereditary Ocular Diseases
arizona.edu

https://disorders.eyes.arizona.edu/handouts/knobloch-syndrome-1

WEBKnobloch syndrome is a rare hereditary disorder of the brain and eyes first described in 1971. Clinical Correlations: The brain may not be properly formed and in many patients the rear of the skull is not fully closed with a sac-like protrusion of brain tissue (occipital encephalocele).

DA: 2 PA: 1 MOZ Rank: 100